Functionalized Erythroid Cells

ABSTRACT

Described herein are novel preparations of functionalized erythroid cells and related compositions, reagents, and methods for use in human pharmaceutical and veterinary applications.

RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 15/932,341, filed Feb. 16, 2018, which claims priority to U.S. Patent Application Ser. No. 62/460,589, filed Feb. 17, 2017, and U.S. Patent Application Ser. No. 62/542,142, filed Aug. 7, 2017, the contents of each of which are incorporated herein by reference in their entirety.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been filed electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Feb. 15, 2018, is named R2081-702110_SL.txt and is 48,634 bytes in size.

BACKGROUND

Erythroid cells such as red blood cells can be engineered to express a wide variety of exogenous therapeutic proteins in order to treat a number of different diseases, as described in WO2015/073587 (Rubius Therapeutics, Inc.). This engineering can involve introducing a transgene into erythroid cell precursors, and then inducing the precursors to differentiate and express the transgene. However, some proteins are difficult to express, e.g., because they require a post-translational modification or because they compromise the growth or function of a host cell. There exists a need for improved methods of producing cells comprising such proteins.

SUMMARY OF THE INVENTION

Described herein are novel preparations of functionalized erythroid cells and related compositions, reagents, and methods that have advantageous and surprising qualities for use in human pharmaceutical and veterinary applications. For example, methods and compositions disclosed herein provide for functionalized erythroid cells having optimized yield, purity, stability, viability, immunogenicity, function, integrity, and/or biological function for use in therapeutic applications. The functionalized erythroid cells described herein are particularly well suited for delivery of agents to the surface of the cells or for complex or difficult to express agents, e.g., polypeptides, e.g., multimeric polypeptides; large polypeptides; agents derivatized in vitro, e.g., polypeptides; agents that may be toxic to, or which cannot be expressed efficiently in, the erythroid cells. The agent may also be a lipid, nucleic acid, sugar, drug, or small molecule.

The methods and compositions disclosed herein provide optimized erythroid cells derivatized with therapeutic or diagnostic agents for use in a broad range of indications. Optimized reagents, intermediates and synthetic methods are also provided.

In one aspect, the invention features a preparation, e.g., pharmaceutical preparation, of erythroid cells, e.g., hematopoietic stem cells, reticulocytes, or erythrocytes, comprising, as many as, at least, more than, or about 5,000, 10,000, 50,000, 100,000, 200,000, 300,000, 400,000, 500,000 coupling reagents per cell. For instance, in some aspects the disclosure features a preparation, e.g., pharmaceutical preparation, of erythroid cells comprising at least 5,000, 10,000, 50,000, 100,000, 200,000, 300,000, 400,000, 500,000 coupling reagents per cell. In some embodiments, a pharmaceutical preparation described herein comprises up to 10,000, 50,000, 100,000, 200,000, 300,000, 400,000, 500,000 coupling reagents per cell. In an embodiment, at least 50, 60, 70, 80, 90, 95, 99, or 99.9% of the cells in the preparation have the recited level of coupling reagent, e.g., an alkyne coupling reagent (KR) per cell or an azide coupling reagent (AR) per cell. In an embodiment at least about 1, 2, 3, 5, 10, 20, 30, or 40% of the cells in the preparation have the recited level of agent per cell. In an embodiment, the preparation comprises, as many as, at least, more than, or about, 10,000, 50,000, 100,000, 10⁶, 10⁷, 10⁸, or 10⁹ cells. In an embodiment, the preparation comprises, as many as, at least, more than, or about, 10¹⁰, 10¹¹, or 10¹² cells. In an embodiment, the cell further comprises a polypeptide expressed from an exogenous nucleic acid, e.g., inside the cell or at the cell surface.

In another aspect, the invention features a preparation, e.g., pharmaceutical preparation, of erythroid cells, e.g., hematopoietic stem cells, reticulocytes, or erythrocytes, comprising, as many as, at least, more than, or about 1,000, 2,000, 3,000, 4,000, or 5,000 coupling reagents per cell. For instance, in some aspects the disclosure features a preparation, e.g., pharmaceutical preparation, of erythroid cells comprising at least 1,000, 2,000, 3,000, 4,000, or 5,000 coupling reagents per cell.

In another aspect, the invention features a preparation, e.g., pharmaceutical preparation, of erythroid cells, e.g., hematopoietic stem cells, reticulocytes, or erythrocytes, comprising, as many as, at least, more than, or about 5,000, 10,000, 50,000, 100,000, 200,000, 300,000, 400,000, 500,000, copies of an agent, e.g., heterologous agent, coupled to the cell by a residual linker. In some embodiments, the residual linker comprises a click signature. For instance, in some aspects the disclosure features a preparation, e.g., pharmaceutical preparation, of erythroid cells comprising at least 5,000, 10,000, 50,000, 100,000, 200,000, 300,000, 400,000, 500,000, copies of a heterologous agent, coupled to the cell by residual linker comprising a click signature.

In an embodiment at least about 50, 60, 70, 80, 90, 95, 99, or 99.9% of the cells in the preparation have the recited level of agent per cell. In an embodiment at least about 50, 60, 70, 80, 90, 95, 99, or 99.9% of the cells in the preparation comprise a first agent and a second agent, e.g., wherein a cell is considered positive for an agent if the level of agent is greater than that measured in 99% of otherwise similar unlabeled cells. In an embodiment at least about 1, 2, 3, 5, 10, 20, 30, or 40% of the cells in the preparation have the recited level of agent per cell. In an embodiment the preparation comprises, as many as, at least, more than, or about, 10,000, 50,000, 100,000, 10⁶, 10⁷, 10⁸, or 10⁹ cells. In an embodiment, the preparation comprises, as many as, at least, more than, or about, 10¹⁰, 10¹¹, or 10¹² cells.

In an embodiment, the erythroid cells are reticulocytes, e.g., from in vitro expanded, differentiated and enucleated HSCs. In embodiments, the erythroid cells comprise hematopoietic precursor cells, e.g., CD34+ cells.

In an embodiment, the erythroid cells are erythrocytes, e.g., obtained from blood.

In an embodiment, the erythroid cells are genetically modified, e.g., the cells comprise a polypeptide expressed from an exogenous nucleic acid (e.g., DNA or RNA, e.g., mRNA).

In an embodiment, the erythroid cells are encapsulated, e.g., hypotonically loaded, with an exogenous protein.

In an embodiment, the preparation is free or substantially free of free coupling reagent, unreacted coupling reagent, an organic solvent, a metal (e.g., copper), a catalyst, or unlabeled cells or unmodified cells.

In an embodiment, the agent is an agent described in WO2015/15302; or in WO2015/073587, each of which is hereby incorporated by reference in its entirety.

In an embodiment, the agent comprises a peptidic agent, e.g., a polypeptide, an enzyme, or an antibody. In an embodiment, the peptidic agent comprises a cytokine, a receptor, a ligand, a hormone, a growth factor, a blood factor, a lysosomal storage enzyme, asparaginase, or a fragment of any of the foregoing comprising an extracellular domain, counterligand binding domain, or other biologically active domain, or a fragment or variant thereof. In an embodiment, the agent comprises an antigen, e.g., a tumor antigen, and infectious disease antigen, and autoantigen.

In an embodiment, the agent comprises a lipid; nucleic acid, e.g. RNA, DNA, siRNA; sugar; drug; or small molecule.

In an embodiment, the agent comprises a polypeptide of greater than about 30, 50, 75, 100, 150, 200, 250, 300, 350, or 400 kilodaltons. In an embodiment, the agent comprises a polypeptide of about 1-2, 1-5, 2-5, 5-10, 10-20, 20-50, 50-100, 100-200, or 200-500 kDa. In an embodiment, the agent comprises a polypeptide of greater than 10, 15, 20, 25, 30, 40, 50, 100, 200, 300, 400, or 500 amino acids.

In an embodiment, the agent, e.g., a polypeptide, comprises post-translational modification, e.g., a post-translational modification that is not made by erythroid cells, or made inefficiently by erythroid cells. In embodiments, the polypeptide, e.g., an antibody, comprises one or more disulfide bridges. In embodiments, the agent, e.g., a polypeptide, lacks a post-translational modification or comprises the modification at a lower level than the protein produced by a mammalian cell, e.g., a CHO cell. In embodiments, the polypeptide (e.g., an antibody) undergoes deglycosylation. In embodiments, the deglycosylation leads to lower ADCC induction and/or lower interaction with Fc gamma receptors.

In some embodiments, the agent, e.g., a polypeptide, does not comprise a post-translational modification that is ordinarily present if the polypeptide is produced in a human cell, e.g., a human erythroid cell. In some embodiments, the agent, e.g., polypeptide, comprises a post-translational modification at a lower level than is ordinarily present if the polypeptide is produced in a human cell, e.g., at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% lower.

In some embodiments, a polypeptide agent comprises one or more non-canonical amino acids. The non-canonical amino acid may be, for example, p-methoxyphenylalanine (pMpa); p-acetylphenylalanine (pApa); p-benzoylphenylalanine (pBpa); p-iodophenylalanine (pIpa); p-azidophenylalanine (pAzpa); p-propargyloxyphenylalanine (pPpa); α-aminocaprylic acid; o-nitrobenzylcysteine (o-NBC); 1,5-dansylalanine; and o-nitrobenzylserine (o-NBS).

In an embodiment, the agent, e.g., a polypeptide, is toxic to, or compromises the growth, function, life span, or development of an erythroid cell. In embodiments, an agent that is toxic to a cell is an agent (e.g., enzyme) that produces a metabolite toxic to the cell.

In an embodiment, the agent comprises a multimeric polypeptide, e.g., a dimer, e.g., a homodimer or heterodimer, a trimer, e.g., a homotrimer or heterotrimer, or a tetramer, e.g., a homotetramer or heterotetramer, e.g., an antibody or a cell surface receptor, e.g., a receptor for a disease vector, e.g., a virus, a drug, or a toxin.

In an embodiment, the agent comprises a polypeptide, e.g., a multimeric polypeptide, comprising a plurality of cysteine bridges. In an embodiment, the agent comprises a polypeptide, e.g., a multimeric polypeptide, comprising one or more cysteine bridges.

In an embodiment, the agent comprises a difficult to express protein. In embodiments, a difficult to express protein is a protein that comprises a post-translational modification that does not normally occur in erythroid cells. In embodiments, the post-translational modification comprises cleavage by a protease that is not normally expressed in erythroid cells. In embodiments, the difficult to express protein comprises an activated clotting factor, and the protease that activates the clotting factor is not ordinarily expressed in erythroid cells. Exemplary activated clotting factors that are activated by cleavage include Factor Va, VIIa, VIIIa, IXa, Xa, XIa, XIIIa, and thrombin.

In an embodiment, the agent comprises an antibody molecule, e.g., a polypeptide comprising one or more of the following: a) sufficient variable region to bind cognate antigen, e.g., HC CDR1, HC CDR2, and HC CDR3, LC CDR1, LC CDR2, and LC CDR3; b) a heavy chain constant sequence comprising one or more of CH1, CH2, and CH3; c) a functional Fc region; and d) a modified or inactive Fc region, e.g., a mutationally inactivated Fc region or an Fc region having a glycosylation state that impairs Fc activity, e.g., a deglycosylated Fc region. In an embodiment, an antibody is a multispecific antibody, e.g., a bispecific antibody. Examples of antibodies include, but are not limited to, Fab, Fab′, F(ab′)2, Fv fragments, scFv antibody fragments, disulfide-linked Fvs (sdFv), a Fd fragment consisting of the VH and CH1 domains, linear antibodies, single domain antibodies such as sdAb (either VL or VH), camelid VHH domains, multi-specific antibodies formed from antibody fragments such as a bivalent fragment comprising two Fab fragments linked by a disulfide bridge at the hinge region, an isolated epitope binding fragment of an antibody, maxibodies, minibodies, nanobodies, intrabodies, diabodies, triabodies, tetrabodies, v-NAR and bis-scFv. In embodiments, the CDRs are defined according to Kabat et al. (1991), “Sequences of Proteins of Immunological Interest,” 5th Ed. Public Health Service, National Institutes of Health, Bethesda, Md. (“Kabat” numbering scheme), Al-Lazikani et al., (1997) JMB 273, 927-948 (“Chothia” numbering scheme), or a combination thereof.

In an embodiment, the agent comprises an antibody, e.g., an IgA, IgG, IgG1, IgG2, IgM, IgE, or IgD.

In an embodiment, the agent comprises an anti-PDL1 antibody molecule, an anti 4-1BB antibody molecule, or an anti-α4β7 antibody molecule. In an embodiment, the agent comprises an anti-PDL1 antibody, an anti 4-1BB antibody, anti-α4β7 antibody, or protein A/G. In an embodiment, the agent comprises 4-1BBL, Factor VIIa, Factor Xa, asparaginase, IL-10, or MOG peptide. In an embodiment, the agent comprises asparaginase and the asparaginase activity of the cells is about 1×10⁻¹²-1×10⁻⁹ U/cell, 1×10⁻¹²-1×10⁻¹¹ U/cell, 1×10⁻¹¹-1×10⁻¹⁰ U/cell, or 1×10⁻¹⁰-1×10⁻⁹ U/cell.

In another aspect, the invention features a preparation, e.g., pharmaceutical preparation, of erythroid cells, e.g., hematopoietic stem cells, reticulocytes, or erythrocytes, comprising: as many as, at least, more than, or about 1,000, 2,000, 3,000, 4,000, 5,000, 10,000, 50,000, 100,000, 200,000, 300,000, 400,000, or 500,000 copies of a first agent, e.g., a heterologous agent, coupled to the cell by a residual linker; and as many as, at least, more than, or about 1,000, 2,000, 3,000, 4,000, 5,000, 10,000, 50,000, 100,000, 200,000, 300,000, 400,000, or 500,000, copies of a second agent, e.g., a heterologous agent, coupled to the cell by a second residual linker. For instance, in some aspects, the disclosure features a preparation, e.g., pharmaceutical preparation, of erythroid cells, comprising at least 1,000 copies of a first heterologous agent, coupled to the cell by a residual linker having a click signature; and at least 1,000 copies of a second heterologous agent, coupled to the cell by a second residual linker having a second click signature. In an embodiment, the first and second residual linkers have different structures. In an embodiment, the first and second residual linkers have the same structure. In an embodiment, the first and second residual linkers have the same structures but have the opposite orientation. In embodiments, the first click signature is different from the second click signature. In some embodiments, the cell comprises at least 2,000 copies of the first heterologous agent and at least 2,000 copies of the second heterologous agent. In some embodiments, the cell comprises at least 5,000 copies of the first heterologous agent and at least 5,000 copies of the second heterologous agent. In some embodiments, the cell comprises at least 10,000 copies of the first heterologous agent and at least 10,000 copies of the second heterologous agent. In some embodiments, the cell comprises at least 50,000 copies of the first heterologous agent and at least 50,000 copies of the second heterologous agent. In some embodiments, the cell comprises at least 100,000 copies of the first heterologous agent and at least 100,000 copies of the second heterologous agent.

In an embodiment, at least about 1, 2, 3, 5, 10, 20, 30, 40, 50, 60, 70, 80, 90, 95, 99, or 99.9% of the cells in the preparation have the recited level of agents per cell. In an embodiment the preparation comprises, as many as, at least, more than, or about 10,000, 50,000, 100,000, 10⁶, 10⁷, 10⁸, 10⁹, 10¹⁰, 10¹¹, or 10¹² cells. In an embodiment the preparation comprises at least 10,000, 50,000, 100,000, 10⁶, 10⁷, 10⁸, 10⁹, 10¹⁰, 10¹¹, or 10¹² cells.

In an embodiment, the erythroid cells further comprise one or more additional agent, e.g., an Nth agent, where N is at least 3, 4, 5, 6, 7, 8, 9, 10, 50, 100, or 200 agents, wherein for each additional agent the cell comprises as many as, at least, more than, or about 1,000, 2,000, 3,000, 4,000, 5,000, 10,000, 50,000, 100,000, 200,000, 300,000, 400,000, or 500,000, copies of the additional agent, e.g., a heterologous agent, coupled to the cell by a residual linker.

In an embodiment, a preparation, e.g., pharmaceutical preparation, disclosed herein is free or substantially free of free coupling reagent, unreacted coupling reagent, an organic solvent, a metal (e.g., copper), a catalyst, or unlabeled cells or unmodified cells.

In an embodiments, in a cell or preparation, e.g., pharmaceutical preparation, disclosed herein, less than 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90% of the coupling reagent on the cell is unreacted coupling reagent. In an embodiments, in a cell or preparation, e.g., pharmaceutical preparation, disclosed herein, less than 15%, 14%, 13%, 12%, 11%, or 10% of the coupling reagent on the cell is unreacted coupling reagent.

In an embodiment, the agent comprises a peptidic agent, e.g., a polypeptide, a protein drug, an enzyme, an antibody (e.g., an scFv), a cytokine, a cytokine receptor, a receptor molecule, a ligand, a hormone, a growth factor, a blood factor, a lysosomal storage enzyme, asparaginase, an antigen (e.g., a tumor antigen, an infectious disease antigen, or autoantigen), or an immune stimulatory molecule (e.g., a costimulatory molecule). In embodiments, the antibody comprises a whole antibody, a fragment thereof, single-chain antibody, humanized antibody; murine antibody; chimeric, mouse-human, mouse-primate, primate-human monoclonal antibody, anti-idiotype antibody, antibody fragments, such as, e.g., scFv, (scFv)2, Fab, Fab′, and F(ab′)2, F(ab1)2, Fv, dAb, and Fd fragments, diabodies, and an antibody-related polypeptide.

In another aspect, the invention features a method of making a pharmaceutical preparation, product, or intermediate comprising: a) coupling a first coupling reagent, e.g., a GMP grade coupling reagent, to an erythroid cell, thereby making a pharmaceutical preparation, product, or intermediate. In an embodiment, the method further comprises: b) contacting the cell with an agent coupled to a second coupling reagent, e.g., a GMP grade coupling reagent, e.g., under conditions suitable for reaction of the first coupling reagent with the second coupling reagent. In embodiments, the method comprises coupling the second coupling reagent to the agent, e.g., before or after step a). In embodiments, the intermediate of step a) is stored before the contacting of step b). In embodiments, the agent coupled to a second coupling reagent is stored before the contacting of step b).

In an embodiment, the method comprises providing a population of erythroid cells for coupling in a). In an embodiment, the method comprises reducing or minimizing entities in the preparation that react with the first coupling reagent. In an embodiment, the method comprises treating, e.g., washing the cell to remove unbound material, e.g., protein, from the cell, e.g., capable of reacting with the first coupling reagent.

In an embodiment, a second agent is coupled to the cell, wherein the method comprises: c) coupling a second coupling reagent, e.g., a GMP grade coupling reagent to an erythroid cell, and d) contacting the cell with a second agent coupled to a second coupling reagent, e.g., a GMP grade coupling reagent, e.g., under conditions suitable for reaction of the first coupling reagent with the second coupling reagent.

In embodiments, the method comprises:

a) coupling a first coupling reagent to the cell,

b) contacting the cell with a first agent coupled to a second coupling reagent which is capable of reacting with the first coupling reagent,

c) coupling a third coupling reagent to the cell, and

d) contacting the cell with a second agent coupled to a fourth coupling reagent which is capable of reacting with the third coupling reagent.

In embodiments, steps a), b), c), and d) are carried out in one of the following orders:

a), then b), then c), and then d);

a), then c), then b), and then d);

a), then c), then d), and then b);

a), then c), then b) and d) simultaneously;

c), then d), then a), and then b);

c), then a), then b), and then d);

c), then a), then d), and then b);

c), then a), then b) and d) simultaneously;

a) and c) simultaneously, then b), and then d);

a) and c) simultaneously, then d), and then b); or

a) and c) simultaneously, then b) and d) simultaneously.

In an embodiment, the conjugation efficiency of the coupling reaction is greater than 50%, 60%, 70%, 80%, 85%, 90%, 95%, 97%, or 98%.

In an embodiment, the erythroid cells are reticulocytes, e.g., from in vitro expanded, differentiated and enucleated HSCs.

In an embodiment, the erythroid cells are erythrocytes, e.g., obtained from blood.

In an embodiment, the erythroid cells are genetically modified, e.g., the cells comprise a polypeptide expressed from an exogenous nucleic acid (e.g., DNA or RNA, e.g., mRNA).

In an embodiment, the erythroid cells are encapsulated, e.g., hypotonically loaded, with an exogenous protein, an agent that binds to a cellular protein, DNA, or RNA.

In some embodiments, an enucleated cell described herein is a reticulocyte, an erythrocyte, or a platelet.

In another aspect, the invention features a method of administering an agent to a subject, e.g., treating a subject, comprising administering a preparation, a composition, or cells described herein to the subject, thereby administering an agent to the subject, e.g., treating the subject. In an embodiment, the method comprises, providing, e.g., by making, or obtaining from another entity, the preparation, composition, or cells. In another aspect, the invention features a cell (e.g., enucleated erythroid cell) described herein, for use in treating a disease or disorder, e.g., a disease or disorder described herein. In another aspect, the invention features the a cell (e.g., enucleated erythroid cell) described herein, for the manufacture of a medicament for treating a disease or disorder, e.g., a disease or disorder described herein.

In an embodiment, the cells are allogeneic to the subject.

In an embodiment, the cells are autologous to the subject.

In an embodiment, an agent is coupled to the cells. In an embodiment, the agent comprises a peptidic agent, e.g., a polypeptide, an enzyme, or an antibody. In an embodiment, the agent comprises a cytokine, a receptor, a ligand, a hormone, a growth factor, a blood factor, a lysosomal storage enzyme, asparaginase, or a fragment of any of the foregoing comprising an extracellular domain, counterligand binding domain, or other biologically active domain.

In an embodiment, less than 7, 6, 5, 4, 3, 2, or 1 day elapses between coupling an agent to the cells and administering the cells to the subject.

In an embodiment, the cells are autologous and less than 7, 6, 5, 4, 3, 2, or 1 day elapses between removal of the cell from the subject and administering the cells to the subject.

In an embodiment, at least 1, 2, 3, 4, 5, 6, 7, 14, 21, or 28 days elapse between removal of the cell from a subject and administering the cells to a subject (e.g., the same or a different subject).

In an embodiment, the method comprises evaluating the subject, and responsive to the evaluation, selecting an agent for coupling to the cell.

In embodiments, a coupling step occurs in vivo or ex vivo. For instance, in embodiments, a coupling agent is administered to a subject under conditions that allow the coupling reagent to couple to a cell, e.g., an erythroid cell. In some embodiments, an agent coupled to a second coupling reagent is administered to a subject under conditions that allow the agent to couple to a cell, e.g., an erythroid cell.

In another aspect, the invention features a method of providing a preparation, composition, or cells comprising: receiving from an entity the identity of an agent, e.g., an agent suitable for the treatment of a subject, and coupling the agent to a cell by a method described herein, thereby providing a preparation, composition, or cells.

In another aspect, the invention features a kit comprising one or more of the following: a) optionally, an erythroid cell; b) a first coupling reagent; c) a second coupling reagent; d) an agent; e) optionally, an erythroid cell coupled to a coupling reagent; f) an agent coupled to a coupling reagent; or g) a reagent for detecting the presence of any of a-f.

In an embodiment the kit comprise one or more of b, c, d, f and g.

In some aspects, the invention features a kit comprising: a) an activated cell (e.g., erythroid cell), b) a first activated agent, c) a second activated agent, and d) optionally a third or further activated agents.

In some aspects, the invention features a method of making a functionalized cell (e.g., a functionalized cell described herein), comprising: a) receiving instructions from a third party (e.g., a doctor, doctor's office, or hospital) to provide a functionalized cell having one or more specified agents, b) contacting an activated cell with an agent or a plurality (e.g., 2, 3, 4, 5, 10, 20, or more) different agents, thereby making the functionalized cell, and c) providing the functionalized cell to the third party.

In some aspect, the invention features a method of obtaining a functionalized cell (e.g., a functionalized cell described herein), comprising: a) transmitting instructions to a third party (e.g., a laboratory) to provide a functionalized cell having one or more specified agents, b) receiving the functionalized cell from the third party, and c) administering the functionalized cell to a subject in need thereof.

In some aspects, the disclosure features a cell (e.g., an erythroid cell and/or an enucleated cell, e.g., an enucleated erythroid cell), comprising:

an agent (e.g., an exogenous polypeptide) at the cell surface, and

a linker, e.g., a residual linker, covalently linking the agent to the cell surface (e.g., to a polypeptide or carbohydrate at the cell surface), wherein the residual linker comprises a click signature.

In some embodiments, the click signature was formed as the product of a click reaction. In some embodiments, the click signature has the structure of a click signature described herein.

The disclosure provides, in some aspects, a cell (e.g., an erythroid cell and/or an enucleated cell, e.g., an enucleated erythroid cell), comprising an exogenous polypeptide agent covalently linked to the cell surface by a residual linker comprising a click signature, via an amino acid side chain of a protein comprised by the cell, e.g., a protein at the cell surface, wherein the click signature was formed as the product of a click reaction or has the structure of a click signature, e.g., a click signature described herein.

The disclosure provides, in some aspects, a cell (e.g., an erythroid cell and/or an enucleated cell, e.g., an enucleated erythroid cell), comprising:

a plurality of exogenous polypeptide agents, each exogenous polypeptide agent of the plurality being covalently linked to the cell surface by a residual linker comprising a click signature,

wherein at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 99% of exogenous polypeptide agents on the cell are linked via an amino acid side chain to a protein comprised by the cell, e.g., a protein at the cell surface,

wherein the click signature was formed as the product of a click reaction or has the structure of a click signature, e.g., a click signature described herein.

In some aspects, the disclosure provides an enucleated erythroid cell, comprising a plurality of copies of an exogenous polypeptide agent covalently linked to the cell surface by a residual linker comprising a click signature, wherein the click signature was formed as the product of a click reaction or has the structure of a click signature, wherein one or more of List 1 herein applies. In some embodiments, the cell lacks a sortase transfer signature. In some embodiments, the cell does not comprise a sortase transfer signature covalently linked to the click signature.

In some aspects, the disclosure provides an enucleated erythroid cell, comprising a plurality of copies of an exogenous polypeptide agent covalently linked to the cell surface by a residual linker comprising a click signature, wherein the click signature was formed as the product of a click reaction or has the structure of a click signature, wherein at least 50%, 60%, 70%, 80%, or 90% of the plurality of exogenous polypeptide agents have the same orientation relative to the cell surface. In some embodiments, the cell lacks a sortase transfer signature. In some embodiments, the cell does not comprise a sortase transfer signature covalently linked to the click signature. In some embodiments, the cell is not genetically engineered, e.g., does not comprise a polypeptide that was expressed from an exogenous nucleic acid. In other embodiments, the cell is genetically engineered, e.g., comprises a polypeptide that was expressed from an exogenous nucleic acid. In some embodiments, the cell does not comprise a non-natural amino acid. In some embodiments, the cell does not comprise a transmembrane protein having a non-natural amino acid.

In some embodiments, the exogenous polypeptide agent comprises a it-clamp. In some embodiments, the exogenous polypeptide agent is covalently linked to the enucleated erythroid cell via the it-clamp. In some embodiments, the exogenous polypeptide agent comprises a ncAA. In some embodiments, the exogenous polypeptide agent is covalently linked to the enucleated erythroid cell via the ncAA. In some embodiments, the exogenous polypeptide agent comprises two or more cysteine residues. In some embodiments, the exogenous polypeptide agent is covalently linked to the enucleated erythroid cell via the two or more cysteine residues, e.g., via a ThioLinker.

In some embodiments, the exogenous polypeptide agent is a peptide ligand that binds a binding partner.

In some embodiments, the cell further comprises a second agent, e.g., a second exogenous polypeptide agent, e.g., wherein the second exogenous polypeptide agent is covalently linked to the cell surface by a second residual linker comprising a click signature. In some embodiments, the cell further comprises a third agent, e.g., a third exogenous polypeptide agent, e.g., wherein the third exogenous polypeptide agent is covalently linked to the cell surface by a second residual linker comprising a click signature.

In some embodiments, the agent, e.g., exogenous polypeptide agent, is covalently linked to an endogenous molecule of the cell, e.g., an endogenous polypeptide at the cell surface.

In some embodiments, at least 50%, 60%, 70%, 80%, or 90% of the exogenous polypeptide agents are covalently linked to the cell surface with a preselected orientation, e.g., are attached by the same moiety or moieties of the exogenous polypeptide agents (e.g., an N-terminus, a C-terminus, or a particular residue, e.g., a particular ncAA, or a particular plurality of residues, e.g., two cysteine residues). In some embodiments of the preparations described herein, at least 50%, 60%, 70%, 80%, or 90% of the exogenous polypeptide agents in the preparation are covalently linked to an enucleated erythroid cell surface with a preselected orientation, e.g., are attached by the same moiety or moieties of the exogenous polypeptide agents (e.g., an N-terminus, a C-terminus, or a particular residue, e.g., a particular ncAA, or a particular plurality of residues, e.g., two cysteine residues).

In some embodiments, the agent, e.g., exogenous polypeptide agent is covalently linked to an endogenous molecule of the cell, e.g., an endogenous polypeptide at the cell surface. In some embodiments, the linker connects the agent to an endogenous molecule of the cell, e.g., an endogenous polypeptide or sugar at the cell surface. In some embodiments, the linker connects the agent to an exogenous molecule of the cell, e.g., an exogenous polypeptide or sugar at the cell surface.

In some embodiments, the click signature comprises a cyclic moiety, e.g., a heterocycle such as triazole e.g., a disubstituted triazole, or a cycloadduct. In some embodiments, the click signature comprises a cycloalkene such as cyclohexene, an alkyl sulfide, a dihydropyrazine such as a 1,2-dihydropyrazine, a diazole, or a sulfur-containing ring such as a thiopyran.

In some embodiments, the click signature was formed by or is capable of being formed by cycloaddition (e.g., a 1,3-dipolar cycloaddition or hetero-Diels-Alder cycloaddition), nucleophilic ring-opening (e.g., openings of strained heterocyclic electrophiles such as aziridines, epoxides, cyclic sulfates, aziridinium ions, and episulfonium ions), carbonyl chemistry of non-aldol type (e.g., formation of ureas, thioureas, hydrazones, oxime ethers, amides, or aromatic heterocycles), or an addition to a carbon-carbon multiple bond (e.g., epoxidation, aziridination, dihydroxylation, sulfenyl halide addition, nitosyl halide addition, or Michael addition).

In some aspects, the disclosure features a method of making (e.g., manufacturing) a cell (e.g., an erythroid cell, e.g., an enucleated erythroid cell), functionalized with an agent comprising:

(a) providing an activated cell comprising a cell bound, e.g., covalently bound, to a first coupling moiety, e.g., a first click handle,

(b) providing an activated agent comprising an agent (e.g., an exogenous polypeptide) bound, e.g., covalently bound, to a second coupling moiety capable of reacting with the first coupling moiety, e.g., a second click handle capable of reacting with the first click handle, and

(c) contacting the activated cell with the activated agent, thereby producing a cell functionalized with the agent.

In embodiments, the method comprises contacting a cell with a first coupling reagent which comprises the first coupling moiety e.g., first click handle, thereby producing the activated cell. In embodiments, the method comprises contacting the agent with a second coupling reagent which comprises the second coupling moiety, e.g., second click handle, thereby producing the activated agent. In embodiments, the method comprises synthesizing the agent to contain the second coupling moiety, e.g., second click handle, e.g., through incorporation of a non-canonical amino acid. In embodiments, the method comprises making a cell comprising a first coupling moiety, e.g., through incorporation of a non-canonical amino acid comprising the first coupling moiety or through incorporation of a sugar (e.g., into a carbohydrate) comprising the first coupling moiety.

In embodiments, contacting the cell with the first coupling reagent occurs before or after contacting the agent with the second coupling reagent. In embodiments, contacting the cell with the first coupling reagent and contacting the agent with the second coupling reagent occur at the same time, e.g., begin at the same time, end at the same time, or have partial overlap.

In embodiments, the first coupling reagent is membrane impermeable. In embodiments, the second coupling reagent is membrane impermeable. In embodiments, the first coupling reagent is membrane permeable. In embodiments, the second coupling reagent is membrane permeable.

In some aspects, the disclosure features a cell, e.g., an erythroid cell, e.g., an enucleated erythroid cell, produced by a method herein. In some embodiments, the method comprises (a) providing an activated cell comprising a cell covalently bound to a first click handle, (b) providing an activated agent comprising an agent (e.g., an exogenous polypeptide) covalently bound to a second click handle capable of reacting with the first click handle, and (c) contacting the activated cell with the activated agent, thereby producing a cell functionalized with the agent.

In some aspects, the disclosure features a method of treating a disease, comprising administering a functionalized cell described herein to a subject in need thereof.

In some embodiments, the first coupling reagent comprises a first substrate-reactive moiety that reacts with one of the following moieties on the agent:

-   -   a) a primary amine (—NH₂) e.g., in a lysine or N-terminus,     -   b) carboxyl (—COOH) e.g., in an aspartic acid, glutamic acid, or         C-terminus,     -   c) sulfhydryl (—SH) e.g., in cysteine, or     -   d) carbonyl (—CHO) e.g., a ketone or aldehyde group e.g. in a         glycoprotein e.g., an oxidized glycoprotein.

In some embodiments, the second coupling reagent comprises a first substrate-reactive moiety that reacts with one of the following moieties on the cell (e.g., a moiety of a protein or carbohydrate on the cell):

-   -   a) a primary amine (—NH₂) e.g., in a lysine or N-terminus,     -   b) carboxyl (—COOH) e.g., in an aspartic acid, glutamic acid, or         C-terminus,     -   c) sulfhydryl (—SH) e.g., in cysteine, or     -   d) carbonyl (—CHO) e.g., a ketone or aldehyde group e.g., in a         glycoprotein, e.g., an oxidized glycoprotein.

In some embodiments, the first substrate-reactive moiety and the second substrate-reactive moiety react with the same type of moiety, e.g., the first substrate-reactive moiety reacts with a first primary amine and the second substrate-reactive moiety reacts with a second primary amine. In some embodiments, the first substrate-reactive moiety and the second substrate-reactive moiety react with different types of moiety.

In some embodiments, the first or second coupling reagent comprises a sortase recognition site e.g., an N-terminal GGG or a C-terminal LPXTG (SEQ ID NO: 1).

In some embodiments, the coupling reagent (e.g., first or second coupling reagent) comprises a click handle. In embodiments, the click handle comprises an alkyne, e.g., a strained alkyne, e.g., a cyclooctyne, e.g., DBCO-sulfo-NHS ester. In some embodiments, the click handle comprises an azide, e.g., a 3-azidopropionic acid sulfo-NHS ester.

In some embodiments, a method herein further comprises contacting the functionalized cell with a terminating reagent which comprises only one coupling moiety, e.g., one click handle. In embodiments, the terminating reagent can react with un-reacted click handles on the cell, thereby reducing the number of un-reacted click handles on the cell. In embodiments, the terminating reagent can react with un-reacted click handles on the agent, thereby reducing the number of un-reacted click handles on the agent. In embodiments, the method comprises sequentially, in either order, contacting the functionalized cell with a terminating reagent can react with un-reacted click handles on the cell and contacting the functionalized cell with a terminating reagent can react with un-reacted click handles on the agent. In embodiments, un-reacted terminating reagent is washed away between the two contacting steps. In embodiments, the terminating reagent has a lower molecular weight and/or lower steric hindrance than the agent. In embodiments, the terminating reagent comprises a detectable label. In some embodiments, the terminating reagent with a detectable label is contacted with an aliquot of a batch of functionalized cells. In some embodiments, if the amount of detectable label that reacts with the functionalized cell is below a predetermined threshold, the batch is approved or released. In some embodiments, if the amount of detectable label that reacts with the functionalized cell is above a predetermined threshold, the batch is withheld or subjected to further processing, e.g., is contacted with a terminating reagent. In embodiments, the terminating reagent comprises an azide or an alkyne group. In embodiments, once the terminating reagent reacts with an agent or cell, it is not substantially reactive, e.g., no more reactive than the N-terminus of wild-type human glycophorin A.

In some embodiments, at least 70%, 80%, 90%, 95%, 97%, 98%, 99%, 99.5%, 99.5%, 99.8%, or 99.9% of the enucleated erythroid cells are labeled, e.g., wherein a cell is considered labeled if the level of agent is greater than that measured in 99% of otherwise similar unlabeled cells.

In some embodiments, the enucleated erythroid cells are labeled with an average of (or an enucleated erythroid cell described herein is labeled with) 50-200,000 copies per cell of the agent, e.g., 50-100, 100-200, 200-500, 500-1,000, 1,000-2,000, 2,000-5,000, 5,000-10,000, 10,000-20,000, 20,000-50,000, 50,000-100,000, or 100,000-200,000 copies per cell of the agent, or with at least 50, 100, 200, 500, 1,000, 2,000, 5,000, 10,000, 20,000, 50,000, 100,000, or 200,000 copies per cell of the agent, or with up to 50, 100, 200, 500, 1,000, 2,000, 5,000, 10,000, 20,000, 50,000, 100,000, or 200,000 copies per cell of the agent.

In some embodiments, at least 10⁷, 10⁸, or 10⁹ enucleated erythroid cells are labeled.

In some embodiments, the population of enucleated erythroid cells are labeled with at least 1, 2, 5, 10, 20, 50, 100, 200, or 500 ng of the agent, e.g., exogenous polypeptide.

In some embodiments, the linked polypeptide agent comprises anti-PD-L1, anti-α4β7, anti-m41BBL, 4-1BBL, Factor VIIa, Factor Xa, asparaginase, or MOG peptide.

In some embodiments, at least 50, 60, 70, 80, 95, 90, 95, 96, 97, 98, or 99% of the labeled erythroid cells bind a ligand, e.g., in a flow cytometry assay of Example 6. In some embodiments, at least 50, 60, 70, 80, 95, 90, 95, 96, 97, 98, or 99% of the enucleated erythroid cells comprise an agent that binds a ligand, e.g., in a flow cytometry assay of Example 6. In embodiments, the cell is considered to bind the ligand by a flow cytometry assay of Example 6 if it has a signal greater than that measured in 99% of otherwise similar cells that lack the agent.

In embodiments, the agent is linked (e.g., adjacently linked with no intervening atoms, or having one or more atoms between the agent and endogenous polypeptide) to an amino acid of an endogenous polypeptide. In embodiments, the linker has a length of at least 5, 10, 20, 30, 40 50, 60, 70, 80, 90, or 100 nm. In embodiments, the linker has a length of about 30-100, 40-90, 50-80, or 60-70 nm. In embodiments, the linker has a length such that the agent is outside of the glycocalyx of the erythroid cell. In some embodiments, the linker comprises PEG, e.g., PEG having a length of about 3-20, e.g., 4-13, e.g., about 4, 5, 12, or 13. In some embodiments, the length of the PEG component is between about 30-60 Angstroms, e.g., 30-40, 40-50, or 50-60 Angstroms. In some embodiments, the linker comprises PEG having a length of about 50-200, 200-400, 400-600, 600-800 or 800-1000 Angstroms.

In some embodiments one or more of List 1 applies, wherein List 1 is:

-   -   a) the agent is linked (e.g., via a residual linker) to an amino         acid other than a glycine of an endogenous membrane protein,         e.g., is linked to at least one non-glycine residue;     -   b) the agent is linked (e.g., via a residual linker) to a site         other than the N-terminus or C-terminus of an endogenous         membrane protein;     -   c) the agent is linked (e.g., via a residual linker) to a site         other than the N-terminus or C-terminus of an membrane protein;     -   d) the agent is linked (e.g., via a residual linker) to a full         length endogenous membrane protein;     -   e) the agent is linked to at least 10, 20, 50, or 100         sequence-distinct polypeptides, e.g., endogenous polypeptides;     -   f) the cell functionalized with an agent lacks a sortase         transfer signature (i.e., a sequence that can be created by a         sortase reaction) such as LPXTG (SEQ ID NO: 1).     -   g) the agent is not linked to a sortase transfer signature,     -   h) at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or         99% of agents on the cell are not linked to a sortase transfer         signature,     -   i) the click signature is not linked to a sortase transfer         signature,     -   j) at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or         99% of click signatures on the cell are not linked to a sortase         transfer signature,     -   k) the agent is not linked to an extracellular sortase transfer         signature;     -   l) at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or         99% of agents on the cell are not linked to an extracellular         sortase transfer signature,     -   m) the click signature is not linked to an extracellular sortase         transfer signature,     -   n) at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or         99% of click signatures on the cell are not linked to an         extracellular sortase transfer signature,     -   o) the agent is not linked to an extracellular sortase transfer         signature that is within 1, 2, 3, 4, 5, 10, 20, 50, or 100 amino         acids of a transmembrane segment;     -   p) at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or         99% of agents on the cell are not linked an extracellular         sortase transfer signature that is within 1, 2, 3, 4, 5, 10, 20,         50, or 100 amino acids of a transmembrane segment,     -   q) the click signature is not linked to an extracellular sortase         transfer signature that is within 1, 2, 3, 4, 5, 10, 20, 50, or         100 amino acids of a transmembrane segment,     -   r) at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or         99% of click signatures on the cell are not linked to an         extracellular sortase transfer signature that is within 1, 2, 3,         4, 5, 10, 20, 50, or 100 amino acids of a transmembrane segment,     -   s) the agent is not linked to a sortase transfer signature that         is within 1, 2, 3, 4, 5, 10, 20, 50, or 100 amino acids of the         agent,     -   t) at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or         99% of agents on the cell are not linked to a sortase transfer         signature that is within 1, 2, 3, 4, 5, 10, 20, 50, or 100 amino         acids of the agent,     -   u) the click signature is not linked to a sortase transfer         signature that is within 1, 2, 3, 4, 5, 10, 20, 50, or 100 amino         acids of the click signature,     -   v) at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or         99% of click signatures on the cell are not linked to a sortase         transfer signature that is within 1, 2, 3, 4, 5, 10, 20, 50, or         100 amino acids of the click signature,     -   w) the polypeptide, e.g., an endogenous polypeptide, to which         the agent is linked does not have a sortase transfer signature         at a position corresponding to the N or C terminus;     -   x) at least 1%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%,         95%, or 99% of agents on the cell are linked via an amino acid         side chain of a protein comprised by the cell, e.g., a protein         at the cell surface, wherein in an embodiment the side chain is         a side chain of lysine, cysteine, aspartic acid, or glutamic         acid, linked such that at least one atom of an amino acid side         chain is disposed between the agent and the backbone of the         protein,     -   y) the agent is connected to a polypeptide (e.g., endogenous         protein) on the cell surface,     -   z) the functionalized cell was not contacted with a sortase,     -   aa) the functionalized cell does not comprise a sortase transfer         signature that comprises a bond that was formed extracellularly,     -   bb) at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%,         or 99% of click signatures on the cell were produced by reacting         the cell with a coupling reagent, or     -   cc) wherein the cell is made by a method that does not comprise         contacting the cell with a non-natural sugar, e.g., a sugar         comprising a click handle, or a combination thereof.

In some embodiments, the cell comprises over 1,000, 5,000, 5,000, 10,000, 50,000, 100,000, 200,000, 300,000, 400,000, or 500,000, copies of the agent.

In some embodiments:

-   -   i) the agent has a clearance rate wherein at least 20% of the         agent remains in the circulatory system of the subject over 1,         2, 3, 4, 5, 6, or 7 days,     -   ii) the population of cells has a clearance rate wherein at         least 20% of the agent remains in the circulatory system of the         subject over 1, 2, 3, 4, 5, 6, or 7 days,     -   iii) the population of cells has a clearance rate wherein at         least 20% of the functional erythroid cells remain in the         circulatory system of the subject over 1, 2, 3, 4, 5, 6, or 7         days;     -   iv) the agent has a clearance rate wherein at least 20% of the         agent that is in the circulatory system of the subject after 1         day remains in the circulatory system after another 1, 2, 3, 4,         5, 6, 7, 14, or 21 days;     -   iv) the population of cells has a clearance rate wherein at         least 20% of the agent that is in the circulatory system of the         subject after 1 day remains in the circulatory system after         another 1, 2, 3, 4, 5, 6, 7, 14, or 21 days;     -   iv) the population of cells has a clearance rate wherein at         least 20% of the population of cells that is in the circulatory         system of the subject after 1 day remains in the circulatory         system after another 1, 2, 3, 4, 5, 6, 7, 14, or 21 days;

In some embodiments, at least at least 50%, 60%, 70%, 80%, 90%, 95%, 97%, 98%, or 99%, of the erythroid cells of the population are enucleated.

In some embodiments, the cells are not hypotonically loaded cells.

In some embodiments, the enucleated erythroid cell has one or more of the following characteristics:

-   -   a) an osmotic fragility of less than 50% cell lysis at 0.3%,         0.35%, 0.4%, 0.45%, or 0.5% NaCl;     -   b) a cell volume of about 10-200 fL or a cell diameter of         between about 1 micron and about 20 microns, between about 2         microns and about 20 microns, between about 3 microns and about         20 microns, between about 4 microns and about 20 microns,         between about 5 microns and about 20 microns, between about 6         microns and about 20 microns, between about 5 microns and about         15 microns, or between about 10 microns and about 30 microns;     -   c) greater than 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9% or 10% fetal         hemoglobin; or at least about 20, 25, or 30 pg/cell of         hemoglobin; or     -   d) phosphatidylserine content of the outer leaflet is less than         30%, 25%, 20%, 15%, 10%, or 5% as measured by Annexin V         staining.

In some embodiments, the residual linker or click signature is within 1, 2, 5, 10, 20, or 50 atoms of an amino acid (e.g., a canonical amino acid) of a polypeptide on the cell. In some embodiments, the residual linker or click signature is not within 1, 2, 5, 10, 20, or 50 atoms of a carbohydrate moiety of the cell. In some embodiments, the agent is linked to a polypeptide that is not glycosylated. In some embodiments, the agent is linked to an amino acid side chain, N-terminus, or C-terminus of a polypeptide that is glycosylated.

In some embodiments, the residual linker is not within 1, 2, 5, 10, 20, or 50 atoms of a mannose moiety on the cell. In some embodiments, at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 99% of residual linkers or click signatures on the cell are not within 1, 2, 5, 10, 20, or 50 atoms of a mannose moiety on the cell. In some embodiments, the residual linker are linked to at least two (e.g., 3, 4, 5, or more) types of sugar on the cell. For instance, a first residual linker can be within 1, 2, 5, 10, 20, or 50 atoms of a first sugar moiety on the cell, and a second residual linker can be within 1, 2, 5, 10, 20, or 50 atoms of a second sugar moiety on the cell.

In some embodiments, the cell is not genetically engineered.

In some embodiments, the cell does not comprise a non-canonical amino acid. In some embodiments, less than 1%, 0.1%, 0.01%, 0.001%, or 0.0001% of amino acids in the cell are non-canonical amino acids.

The disclosure contemplates all combinations of any one or more of the foregoing aspects and/or embodiments, as well as combinations with any one or more of the embodiments set forth in the detailed description and examples.

Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, suitable methods and materials are described below. All publications, patent applications, patents, and other references (e.g., sequence database reference numbers) mentioned herein are incorporated by reference in their entirety. For example, all GenBank, Unigene, NCBI, and Entrez sequences referred to herein, e.g., in any Table herein, are incorporated by reference. Unless otherwise specified, the sequence accession numbers specified herein, including in any Table herein, refer to the database entries current as of Aug. 7, 2017. When one gene or protein references a plurality of sequence accession numbers, all of the sequence variants are encompassed.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a diagram showing a method of clicking an agent onto a cell. An activated agent can be made, e.g., by contacting an agent with a first coupling reagent having a first substrate reactive moiety and a first coupling moiety which is a click handle, and allowing the first substrate reactive moiety to react with the agent. An activated cell can be made, e.g., by contacting a cell with a second coupling reagent having a second substrate reactive moiety and a second coupling moiety which is a click handle, and allowing the second substrate reactive moiety to react with the cell. The activated agent and activated cell are then combined under conditions that allow the first click handle to react with the second click handle, producing a residual linker comprising a click signature.

FIGS. 2A-2C are flow cytometry images of erythroid cells that have been coupled to an exemplary agent (an anti-α4β7 antibody) using the coupling reagents described herein.

FIG. 3 is a graph showing the percentage of tumor cells bound by erythroid cells functionalized with anti-PD-L1 antibody or control cells functionalized with isotype control antibody.

FIG. 4 is a time course showing tumor size in mice treated with 41BBL-RCT and an untreated control.

FIG. 5 is a graph showing serum asparagine levels over time in C57BL/6 mice treated with RCT-asparaginase.

FIG. 6 is a graph showing serum asparagine levels over time in Rag1−/− mice treated with RCT-asparaginase.

FIGS. 7A and 7B are graphs showing fluorescence over time in mice treated with Cy5-labeled RCT-asparaginase. FIG. 7A, high dose ASNase mRBCs; FIG. 7B, low dose ASNase mRBCs.

FIGS. 8A and 8B are graphs showing the oriented labeling of HIS6 mouse 41BBL using a ThioLinker click handle results in increased functional activity of coupled cells. FIG. 8A, IL-2 secretion; FIG. 8B, interferon-γ secretion.

FIGS. 9A and 9B show site-specific incorporation of a non-canonical amino acid, exo(BCN)-lysine, into mouse 41BBL, to create a clickable mouse 41BBL. FIG. 9A, chemical structure of exo(BCN)-lysine; FIG. 9B, western blot showing that clicked mouse 41BBL was produced at concentrations of exo(BCN)-lysine of 1 mM or above.

DETAILED DESCRIPTION OF THE INVENTION

Described herein are compositions and methods that include functionalization of erythroid cells using selective, biocompatible reactions to couple the cells with an agent (e.g., a peptidic agent) of interest. In some embodiments, the reactions are cycloaddition reactions (e.g., a Huisgen 1,3-dipolar cycloaddition reaction) using reagents that are water-soluble and membrane impermeable.

Definitions

A “click signature,” as that term is used herein, refers to a plurality of atoms disposed between and covalently linking entity A and entity B, wherein the click signature is formed as the product of a click reaction that links entity A and entity B. In an embodiment the click signature has the structure of a click signature that is formed as the product of a click reaction that links entity A and entity B, but is not limited a click signature made by any particular process, e.g., not limited to a click signature formed by a click reaction, but can be formed or provided by another process. In an embodiment, the click signature is an alkyne/azide click signature, e.g., the click signature comprises a triazole.

A “click reaction”, as that term is used herein, refers to a range of reactions used to covalently link a first and a second moiety, for convenient production of linked products. It typically has one or more of the following characteristics: it is fast, is specific, is high-yield, is efficient, is spontaneous, does not significantly alter biocompatibility of the linked entities, has a high reaction rate, produces a stable product, favors production of a single reaction product, has high atom economy, is chemoselective, is modular, is stereoselective, is insensitive to oxygen, is insensitive to water, is high purity, generates only inoffensive or relatively non-toxic byproducts that can be removed by nonchromatographic methods (e.g., crystallization or distillation), needs no solvent or can be performed in a solvent that is benign or physiologically compatible, e.g., water, stable under physiological conditions. Examples include an alkyne/azide reaction, a diene/dienophile reaction, or a thiol/alkene reaction. Other reactions can be used. In some embodiments, the click reaction is fast, specific, and high-yield. For instance, in embodiments, a fast click reaction has a second order forward rate constant of 10-200 M⁻¹s⁻¹, 1-20 M⁻¹s⁻¹, or at least 1, 2, 3, 5, 10, 20, 50, 60, 100, 200, 500, 1E3, 2E3, 5E3, 1E4, 2E4, 5E4, 1E5, 2E5, 5E5, or 1E6 M⁻¹s⁻¹, e.g., at 20° C. in PBS. In some embodiments, a specific click reaction is one in which, when an unmodified cell (e.g., a human red blood cell isolated from peripheral circulation) is contacted with an agent having a click handle, less than 10%, 5%, 4%, 3%, 2%, or 1% of the cells are detectably linked to the agent, e.g., after a reaction time of 1 hour at 20° C. in PBS, e.g., in an assay of Example 21. In some embodiments, a high-yield click reaction is one which has at least 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% yield, e.g., for a reaction time of 1 hour at 20° C. in PBS.

A “click handle,” as that term is used herein, refers to a chemical moiety that is capable of reacting with a second click handle in a click reaction to produce a click signature. In embodiments, a click handle is comprised by a coupling reagent, and the coupling reagent may further comprise a substrate reactive moiety.

As used herein, a “sortase transfer signature” is a sequence that can be created by a sortase reaction that links a first sortase recognition motif with a second sortase recognition motif, wherein the sortase transfer signature comprises the amino acid sequence of the first sortase recognition motif and the amino acid sequence second recognition motif, minus any amino acids (e.g., Gly-Gly) removed during the sortase reaction. For instance, a sortase-mediated reaction of LPXTGG (SEQ ID NO: 2) with (G)_(n) can produce a sortase transfer signature of LPXT(G)_(n) (SEQ ID NO: 1).

Cells

The present invention features compositions comprising functionalized cells and methods of use thereof. In embodiments, the cells comprise erythroid cells. In embodiments, the cell is other than a platelet, platelet precursor, or platelet progenitor. In embodiments, the cells are nucleated or enucleated. In embodiments, the cells are eukaryotic cells, e.g., mammalian cells, e.g., human cells. In embodiments, the cells comprise T cells (e.g., CD4 T cells or CD8 T cells), B cells, natural killer cells, natural killer T cells, Myeloid Cells, Dendritic Cells, Platelets, or Neutrophils. In embodiments, the cells comprise endoderm-derived cells, ectoderm-derived cells, or mesoderm-derived cells. In embodiments, the cells comprise stem cells, mesenchymal stem cells, neural stem cells, cardiomyocytes, cells for allogeneic transplant, cells for xenogeneic transplant, or pancreatic beta cells.

Erythroid Cells

The present invention features compositions comprising functionalized erythroid cells and methods of use thereof “Erythroid cells,” as used herein, are cells of the erythrocytic series including hematopoietic stem cells (HSCs), and nucleated and enucleated red blood cell precursors, enucleated red blood cells, and any intermediates between HSCs and enucleated red blood cells. In an embodiment, an erythroid cell is a proerythroblast, basophilic erythroblast, polychromatophilic erythroblast, orthochromatic erythroblast, reticulocyte, and erythrocyte. In an embodiment, an erythroid cell is a cord blood stem cell, a CD34+ cell, a hematopoietic stem cell (HSC), a spleen colony forming (CFU-S) cell, a common myeloid progenitor (CMP) cell, a blastocyte colony-forming cell, a burst forming unit-erythroid (BFU-E), a megakaryocyte-erythroid progenitor (MEP) cell, an erythroid colony-forming unit (CFU-E), a reticulocyte, an erythrocyte, an induced pluripotent stem cell (iPSC), a mesenchymal stem cell (MSC), a polychromatic normoblast, an orthochromatic normoblast, or a combination thereof.

In embodiments, the erythroid cells are, or are derived from, immortal or immortalized cells. For example, immortalized erythroblast cells can be generated by retroviral transduction of CD34+ hematopoietic progenitor cells to express Oct4, Sox2, Klf4, cMyc, and suppress TP53 (e.g., as described in Huang et al. (2013) _Mol Ther, epub ahead of print September 3).

In embodiments, the erythroid cells may be intended for autologous use or provide a source for allogeneic transfusion. In some embodiments, erythroid cells are cultured. In an embodiment an erythroid cell is an enucleated red blood cell.

In embodiments, an erythroid cell is obtained from a biological sample, e.g., erythrocytes from human blood, or HSCs from bone marrow.

In embodiments, an erythroid cell is obtained from an ex-vivo or in vitro process, e.g., whereby precursor cells, e.g., hematopoietic stem cells (e.g., human hematopoietic stem cells isolated from bone marrow, cytokine-stimulated peripheral blood or umbilical cord blood) are expanded and or differentiated and enucleated ex vivo to produce, e.g., reticulocytes. Ex vivo methods of manufacturing enucleated erythroid cells (e.g., reticulocytes) from stem cells are described, e.g., in Migliaccio and Palis (2011) Drug Discov Today Dis Mech. 8(1-2): e3-e8; WO2015/073587 and WO2015/153102, each of which is incorporated by reference in its entirety. Erythroid cells, e.g., reticulocytes, prepared via this process may be functionalized according to the methods described herein.

In an embodiment an enucleated cell is a cell that has lost its nucleus through differentiation from a precursor cell, e.g., a hematopoietic stem cell (e.g., a CD34+ cell), a common myeloid progenitor (CMP), a megakaryocyte erythrocyte progenitor cell (MEP), a burst-forming unit erythrocyte (BFU-E), a colony-forming unit erythrocyte (CFU-E), a pro-erythroblast, an early basophilic erythroblast, a late basophilic erythroblast, a polychromatic erythroblast, or an orthochromatic erythroblast, or an induced pluripotent cell, into a reticulocyte or mature red blood cell. In an embodiment an enucleated cell is a cell that has lost its nucleus through in vitro differentiation from a precursor cell, e.g., a hematopoietic stem cell (e.g., a CD34+ cell), a common myeloid progenitor (CMP), a megakaryocyte erythrocyte progenitor cell (MEP), a burst-forming unit erythrocyte (BFU-E), a colony-forming unit erythrocyte (CFU-E), a pro-erythroblast, an early basophilic erythroblast, a late basophilic erythroblast, a polychromatic erythroblast, or an orthochromatic erythroblast, or an induced pluripotent cell into a reticulocyte or mature red blood cell.

An erythroid cell used in the functionalization methods described herein may be unmodified or may be modified, e.g., genetically engineered (e.g., genetically engineered to express an exogenous protein); may be encapsulated, e.g., hypotonically loaded, with an exogenous protein. An erythroid cell used in the treatment methods described herein may be autologous, allogeneic, or xenogeneic.

Exemplary cells for use in preparations, compounds, methods and kits described herein are described herein. In an embodiment, the cell, e.g., erythroid cell, e.g., erythrocyte, comprises one or more of the following properties: a) it is obtained from blood, an in vitro culture, or was differentiated from a more primitive cell type in vitro, e.g., a hematopoietic stem cell; b) it has been hypotonically loaded with an agent; or c) it is a genetically engineered erythroid cell, e.g., expressing an exogenous agent, e.g., a polypeptide.

In an embodiment, the cell is differentiated from a more primitive cell type in vitro, e.g., a hematopoietic stem cell.

In an embodiment, the cell is a genetically engineered erythroid cell, e.g., expressing an exogenous agent, e.g., a polypeptide.

In an embodiment, the cell is an erythrocyte obtained from blood.

In an embodiment, the cell has been hypotonically loaded with an agent.

In an embodiment, the cell is from an in vitro culture.

In an embodiment, the cell is a genetically engineered erythroid cell, e.g., expressing an exogenous agent, e.g., a polypeptide.

Physical Characteristics of Enucleated Erythroid Cells

In some embodiments, the enucleated erythroid cells described herein have one or more (e.g., 2, 3, 4, or more) physical characteristics described herein, e.g., osmotic fragility, cell size, hemoglobin concentration, or phosphatidylserine content. While not wishing to be bound by theory, in some embodiments an enucleated erythroid cell described herein has physical characteristics that resemble a wild-type, untreated erythroid cell. In contrast, a hypotonically loaded erythroid cell sometimes displays aberrant physical characteristics such as increased osmotic fragility, altered cell size, reduced hemoglobin concentration, or increased phosphatidylserine levels on the outer leaflet of the cell membrane.

In some embodiments, the erythroid cell is in a composition that lacks a stabilizer.

Osmotic Fragility

In some embodiments, the enucleated erythroid cell exhibits substantially the same osmotic membrane fragility as an isolated, uncultured enucleated erythroid cell. In some embodiments, the population of enucleated erythroid cells has an osmotic fragility of less than 50% cell lysis at 0.3%, 0.35%, 0.4%, 0.45%, or 0.5% NaCl. Osmotic fragility is determined, in some embodiments, using the method of Example 59 of WO2015/073587.

Cell Size

In some embodiments, the enucleated erythroid cell has approximately the diameter or volume as a wild-type, untreated erythroid cell.

In some embodiments, the population of erythroid cells has an average diameter of about 4, 5, 6, 7, or 8 microns, and optionally the standard deviation of the population is less than 1, 2, or 3 microns. In some embodiments, the one or more erythroid cell has a diameter of about 4-8, 5-7, or about 6 microns. In some embodiments, the diameter of the erythroid cell is less than about 1 micron, larger than about 20 microns, between about 1 micron and about 20 microns, between about 2 microns and about 20 microns, between about 3 microns and about 20 microns, between about 4 microns and about 20 microns, between about 5 microns and about 20 microns, between about 6 microns and about 20 microns, between about 5 microns and about 15 microns or between about 10 microns and about 30 microns. Cell diameter is measured, in some embodiments, using an Advia 120 hematology system.

In some embodiment the volume of the mean corpuscular volume of the erythroid cell is greater than 10 fL, 20 fL, 30 fL, 40 fL, 50 fL, 60 fL, 70 fL, 80 fL, 90 fL, 100 fL, 110 fL, 120 fL, 130 fL, 140 fL, 150 fL, or greater than 150 fL. In one embodiment the mean corpuscular volume of the erythroid cell is less than 30 fL, 40 fL, 50 fL, 60 fL, 70 fL, 80 fL, 90 fL, 100 fL, 110 fL, 120 fL, 130 fL, 140 fL, 150 fL, 160 fL, 170 fL, 180 fL, 190 fL, 200 fL, or less than 200 fL. In one embodiment the mean corpuscular volume of the erythroid cells is between 80-100, 100-200, 200-300, 300-400, or 400-500 femtoliters (fL). In some embodiments, a population of erythroid cells has a mean corpuscular volume set out in this paragraph and the standard deviation of the population is less than 50, 40, 30, 20, 10, 5, or 2 fL. The mean corpuscular volume is measured, in some embodiments, using a hematological analysis instrument, e.g., a Coulter counter.

Hemoglobin Concentration

In some embodiments, the enucleated erythroid cell has a hemoglobin content similar to a wild-type, untreated erythroid cell. In some embodiments, the erythroid cells comprise greater than 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9% or greater than 10% fetal hemoglobin. In some embodiments, the erythroid cells comprise at least about 20, 22, 24, 26, 28, or 30 pg, and optionally up to about 30 pg, of total hemoglobin. Hemoglobin levels are determined, in some embodiments, using the Drabkin's reagent method of Example 33 of WO2015/073587.

Phosphatidylserine Content

In some embodiments, the enucleated erythroid cell has approximately the same phosphatidylserine content on the outer leaflet of its cell membrane as a wild-type, untreated erythroid cell. Phosphatidylserine is predominantly on the inner leaflet of the cell membrane of wild-type, untreated erythroid cells, and hypotonic loading can cause the phosphatidylserine to distribute to the outer leaflet where it can trigger an immune response. In some embodiments, the population of erythroid cells comprises less than about 30, 25, 20, 15, 10, 9, 8, 6, 5, 4, 3, 2, or 1% of cells that are positive for Annexin V staining. Phosphatidylserine exposure is assessed, in some embodiments, by staining for Annexin-V-FITC, which binds preferentially to PS, and measuring FITC fluorescence by flow cytometry, e.g., using the method of Example 54 of WO2015/073587.

Other Characteristics

In some embodiments, the population of erythroid cells comprises at least about 50%, 60%, 70%, 80%, 90%, or 95% (and optionally up to 90 or 100%) of cells that are positive for GPA. The presence of GPA is detected, in some embodiments, using FACS.

In some embodiments, the enucleated erythroid cells have a half-life of at least 30, 45, or 90 days in a subject.

In some embodiments, a population of cells comprising erythroid cells comprises less than about 10, 5, 4, 3, 2, or 1% echinocytes.

In some embodiments, an erythroid cell is enucleated. In some embodiments, a cell, e.g., an erythroid cell, contains a nucleus that is non-functional, e.g., has been inactivated.

Universal Donor Erythroid Cells

In some embodiments, erythroid cells described herein are autologous or allogeneic to the subject to which the cells will be administered. For example, erythroid cells allogeneic to the subject include one or more of blood type specific erythroid cells (e.g., the cells can be of the same blood type as the subject) or one or more universal donor erythroid cells. In some embodiments, the enucleated erythroid cells described herein have reduced immunogenicity compared to a reference cell, e.g., have lowered levels of one or more blood group antigens.

Where allogeneic cells are used for transfusion, a compatible ABO blood group can be chosen to prevent an acute intravascular hemolytic transfusion reaction. The ABO blood types are defined based on the presence or absence of the blood type antigens A and B, monosaccharide carbohydrate structures that are found at the termini of oligosaccharide chains associated with glycoproteins and glycolipids on the surface of the erythrocytes (reviewed in Liu et al., Nat. Biotech. 25:454-464 (2007)). Because group O erythrocytes contain neither A nor B antigens, they can be safely transfused into recipients of any ABO blood group, e.g., group A, B, AB, or O recipients. Group O erythrocytes are considered universal and may be used in all blood transfusions. Thus, in some embodiments, an erythroid cell described herein is type O. In contrast, group A erythroid cells may be given to group A and AB recipients, group B erythroid cells may be given to group B and AB recipients, and group AB erythroid cells may be given to AB recipients.

In some instances, it may be beneficial to convert a non-group O erythroid cell to a universal blood type. Enzymatic removal of the immunodominant monosaccharides on the surface of group A and group B erythrocytes may be used to generate a population of group O-like erythroid cells (See, e.g., Liu et al., Nat. Biotech. 25:454-464 (2007)). Group B erythroid cells may be converted using an α-galactosidase derived from green coffee beans. Alternatively or in addition, α-N-acetylgalactosaminidase and α-galactosidase enzymatic activities derived from E. meningosepticum bacteria may be used to respectively remove the immunodominant A and B antigens (Liu et al., Nat. Biotech. 25:454-464 (2007)), if present on the erythroid cells. In one example, packed erythroid cells isolated as described herein, are incubated in 200 mM glycine (pH 6.8) and 3 mM NaCl in the presence of either α-N-acetylgalactosaminidase and α-galactosidase (about 300 μg/ml packed erythroid cells) for 60 min at 26° C. After treatment, the erythroid cells are washed by 3-4 rinses in saline with centrifugation and ABO-typed according to standard blood banking techniques.

While the ABO blood group system is the most important in transfusion and transplantation, in some embodiments it can be useful to match other blood groups between the erythroid cells to be administered and the recipient, or to select or make erythroid cells that are universal for one or more other (e.g., minor) blood groups. A second blood group is the Rh system, wherein an individual can be Rh+ or Rh−. Thus, in some embodiments, an erythroid cell described herein is Rh−. In some embodiments, the erythroid cell is Type O and Rh−.

In some embodiments, an erythroid cell described herein is negative for one or more minor blood group antigens, e.g., Le(a−b−) (for Lewis antigen system), Fy(a−b−) (for Duffy system), Jk(a−b−) (for Kidd system), M−N− (for MNS system), K−k− (for Kell system), Lu(a−b−) (for Lutheran system), and H-antigen negative (Bombay phenotype), or any combination thereof. In some embodiments, the erythroid cell is also Type O and/or Rh−. Minor blood groups are described, e.g., in Agarwal et al “Blood group phenotype frequencies in blood donors from a tertiary care hospital in north India” Blood Res. 2013 March; 48(1): 51-54 and Mitra et al “Blood groups systems” Indian J Anaesth. 2014 September-October; 58(5): 524-528, each of which is incorporated herein by reference in its entirety.

Erythroid Cell Compositions

In some embodiments, the population of erythroid cells comprises at least 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 98% (and optionally up to about 80, 90, or 100%) enucleated erythroid cells. In some embodiments, the population of erythroid cells contains less than 1% live nucleated cells, e.g., contains no detectable live nucleated cells. Enucleation is measured, in some embodiments, by FACS using a nuclear stain. In some embodiments, at least 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, or 80% (and optionally up to about 70, 80, 90, or 100%) of erythroid cells in the population comprise one or more (e.g., 2, 3, 4 or more) of the agents. Presence of the agent is measured, in some embodiments, by FACS using a labeled protein (e.g., antibody) that binds the agent. In some embodiments, at least 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, or 80% (and optionally up to about 70, 80, 90, or 100%) of erythroid cells in the population are enucleated and comprise one or more agents. In some embodiments, the population of erythroid cells comprises about 1×10⁹-2×10⁹, 2×10⁹-5×10⁹, 5×10⁹-1×10¹⁰, 1×10¹⁰-2×10¹⁰, 2×10¹⁰-5×10¹⁰, 5×10¹⁰-1×10¹¹, 1×10¹¹-2×10¹¹, 2×10¹¹-5×10¹¹, 5×10¹¹-1×10¹², 1×10¹²-2×10¹², 2×10¹²-5×10¹², or 5×10¹²-1×10¹³ cells.

Clickable Format Cells

In some embodiments, the cell comprises a conjugation agent without requiring a step of chemically reacting the cell with the conjugation agent. For example, the cell can be contacted with a molecule that comprises a metabolite (e.g., an amino acid or sugar) and a coupling moiety (e.g., a click handle). The cell is then allowed to incorporate the metabolite, e.g., into proteins or carbohydrates, e.g., on the surface of the cell. The metabolite can be, e.g., a non-canonical amino acid. In embodiments, the metabolite is incorporated using a tRNA/amino-acyl-tRNA-synthetase pair that directs the metabolite into a specific position, e.g., one encoded by an Amber stop codon. The resulting activated cell comprises the coupling moiety (e.g., click handle). The activated cell can then be contacted with an activated agent, e.g., an activated agent described herein.

A variety of molecules that comprise a metabolite and a coupling moiety can be used. For instance, in embodiments, the molecule is chosen from:

SCO-Lysine, e.g., for use in a strain-promoted alkyne-azide cycloaddition (SPAAC) reaction;

Cyclopropene lysine, e.g., for use in a strain-promoted inverse-electron-demand Diels-Alder cycloaddition (SPIEDAC) reaction;

TCO*A-Lysine, e.g., for use in a SPIEDAC reaction;

Exo-BCN-Lysine, e.g., for use in a SPAAC reaction;

NBO-Lysine, e.g., for use in a SPIEDAC reaction;

rac-BCN-Lysine, e.g., for use in a SPAAC reaction;

TCO-Lysine, e.g., for use in a SPIEDAC reaction;

Endo-BCN-Lysine, e.g., for use in a SPAAC reaction

PrK-HCL-salt, e.g., for use in a SPAAC or SPIEDAC reaction;

N3-Lysine, e.g., for use in a SPAAC or SPIEDAC reaction

p-acetylphenylalanine, e.g., for use with a site-specific oxime ligation (e.g., mediated by DBCO-amine), followed by SPAAC

p-azidomethylphenylalanine, e.g., for use in a SPAAC or SPIEDAC reaction; or

seleno-cysteine, e.g., for reaction with maleimide.

Coupling Reagents

Described herein are compositions of erythroid cells functionalized with an agent, wherein the cells and the agent are linked through a set of bispecific coupling reagents. In some embodiments, a set of bispecific coupling reagents comprises a first coupling reagent and a second coupling reagent. The first coupling reagent comprises a coupling moiety, e.g., an alkyne moiety, that reacts specifically with the coupling moiety, e.g, an azide, on the second coupling reagent. The coupling moieties do not self-react. In embodiments, the coupling moiety is a click handle. A click handle may comprise an azide or an alkyne.

Each coupling reagent also comprises a substrate reactive moiety, suitable, e.g., for binding (e.g., covalently) to a substrate of interest, e.g., an erythroid cell, or an agent for attachment to an erythroid cell, e.g., a polypeptide, lipid, nucleic acid, sugar, drug, small molecule. In embodiments, the substrate reactive moiety is capable of reacting non-enzymatically with a substrate. In embodiments, the substrate reactive moiety is capable of reacting with a substrate other than in a sortase reaction.

In embodiments, a coupling reagent is capable of covalently linking a first entity (e.g., a cell) with a second entity (e.g., an exogenous polypeptide).

The first coupling reagent can be linked via its substrate reactive moiety to a first substrate, e.g., an erythroid cell. The second coupling reagent can be linked via its substrate reactive moiety to a second substrate, e.g., a polypeptide or drug. The thus derivatized substrates can then be linked to one another.

Linkage of the two substrates typically results in a residual linker between the first and second substrate. For example, in the case of coupling reagents comprising an azide and an alkyne, a residual linker may be formed comprising a triazole (e.g., a 1,2,3-triazole). Exemplary coupling reagents include alkyne coupling reagents (KR) and azide coupling reagents (AR).

In some embodiments, the coupling reagent comprises an alkyne coupling reagent. In some embodiments, the alkyne coupling reagent comprises a propargyl moiety or a cyclooctynyl moiety. Exemplary alkyne coupling reagents include diarylcyclooctyne (DBCO)-sulfo-NHS-ester, diarylcyclooctyne (DBCO)-PEG-NHS-ester, diarylcyclooctyne (DBCO)-C6-NHS-ester, diarylcyclooctyne (DBCO)-NHS-ester, diarylcyclooctyne (DBCO)-amine, diarylcyclooctyne (DBCO)-acid, sulfo diarylcyclooctyne (DBCO)-maleimide, diarylcyclooctyne (DBCO)-maleimide, bis-sulfone-PEG-diarylcyclooctyne (DBCO), propargyl-NHS ester, propargyl-maleimide, alkyne-PEG-NHS ester, alkyne-PEG-maleimide, or a derivative thereof.

In some embodiments, the coupling reagent comprises an azide coupling reagent. In some embodiments, the azide coupling reagent comprises an azidoalkyl moiety, azidoaryl moiety, or an azidoheteroaryl moiety. Exemplary azide coupling reagents include 3-azidopropionic acid sulfo-NHS ester, azidoacetic acid NHS ester, azido-PEG-NHS ester, azidopropylamine, azido-PEG-amine, azido-PEG-maleimide, bis-sulfone-PEG-azide, or a derivative thereof.

Coupling reagents may also comprise an alkene moiety, e.g., a transcycloalkene moiety, an oxanorbornadiene moiety, or a tetrazine moiety. Additional coupling reagents can be found in Click Chemistry Tools (https://clickchemistrytools.com/), Lahann, J (ed) (2009) Click Chemistry for Biotechnology and Materials Science, McKay et al, “Click chemistry in complex mixtures: bioorthogonal bioconjugation” Chem Biol. 2014 Sep. 18; 21(9):1075-101, Becer et al. “Click chemistry beyond metal-catalyzed cycloaddition” Angew Chem Int Ed Engl. 2009; 48(27):4900-8., and Hein et al. “Click chemistry, a powerful tool for pharmaceutical sciences” Pharm Res. 2008 October; 25(10):2216-30, each of which is incorporated herein by reference in its entirety.

In embodiments, the coupling reagent comprises a tetrazine moiety, e.g., for reaction with an alkene moiety. For instance, in embodiments, the tetrazine is a 1,2,4,5 tetrazine and the alkene is a strained alkene. In embodiments, the alkene coupling reagent comprises a trans-cyclooctene, (E)-Cyclooct-4-enol, (E)-Cyclooct-4-enyl 2,5-dioxo-1-pyrrolidinyl carbonate, 5-Norbornene-2-acetic acid succinimidyl ester, 5-Norbornene-2-endo-acetic acid, TCO PEG4 succinimidyl ester, TCO-amine, or TCO-PEG3-maleimide. In embodiments, the tetrazine coupling reagent comprises (4-(1,2,4,5-Tetrazin-3-yl)phenyl)methanamine or 2,5-Dioxo-1-pyrrolidinyl 5-[4-(1,2,4,5-tetrazin-3-yl)benzylamino]-5-oxopentanoate, 5-[4-(1,2,4,5-Tetrazin-3-yl)benzylamino]-5-oxopentanoic acid. In embodiments, the tetrazine and alkene react in a Diels-Alder cycloaddition to yield a stable covalent linkage. In embodiments, a catalyst is not needed. In embodiments, the only byproduct is dinitrogen. In embodiments, the reaction at least one order of magnitude faster than azide-cyclooctyne based click chemistry. Without wishing to be bound by theory, tetrazine/alkene reactions can be used with low concentrations of reactant (e.g., the agent).

In some embodiments, the coupling moieties of each coupling reagent react via an azide-alkyne Huisgen cycloaddition. In some embodiments, an azide-alkyne Huisgen cycloaddition comprises a copper(I)-catalyzed azide-alkyne cycloaddition or a strain-promoted azide-alkyne cycloaddition.

In some embodiments, the coupling moieties of each coupling reagent react to form a heteroaryl, e.g., a triazole. In some embodiments, the triazole comprises a 1,2,3-triazole, e.g., a 1,4-disubstituted 1,2,3-triazole or a 1,5-disubstituted 1,2,3-triazole.

In some embodiments, the coupling reagent comprises a substrate reactive moiety to link the coupling reagent to an agent (e.g., an agent described herein). In some embodiments, the substrate reactive moiety reacts with a carbonyl, an ester, a carboxylic acid, an amine, or a sulfhydryl group. In some embodiments, the substrate reactive moiety comprises a succinimide (e.g., NHS-ester), a maleimide, an amine, a hydrazine, an alkoxyamine, a carboxylic acid, an aldehyde, a ketone, a disulfide, an acyl halide, an isothiocyanate, or a derivative thereof.

In some embodiments, the substrate reactive moiety comprises a linker. In some embodiments, the linker comprises a polyethylene glycol (PEG) moiety. In some embodiments, the linker is a straight chain. In some embodiments, the linker is a branched chain.

In some embodiments, the coupling reagent comprises an alkyne and reacts with an amine. In some embodiments, the coupling agent comprises a cyclooctyne and reacts with an amine. In some embodiments, the coupling agent is diarylcyclooctyne (DBCO)-sulfo-NHS-ester or diarylcyclooctyne (DBCO)-PEG5-NHS-ester.

In some embodiments, the coupling agent comprises an azide and reacts with an amine. In some embodiments, the coupling agent is 3-azidopropionic acid sulfo-NHS ester or azido-PEG4-NHS-ester.

In an embodiment, the coupling reagent is water soluble. In an embodiment, the coupling reagent is membrane impermeable, e.g., has sufficient charge to render it membrane impermeable. In an embodiment the coupling reagent is charged, e.g., positively charged or negatively charged. In an embodiment, the coupling reagent comprises a cationic moiety or an anionic moiety, e.g., a SO₃ moiety.

In some embodiments, the coupling agent comprises a detection agent, e.g., useful for detection of the functionalize erythroid cell. Exemplary detection agents may include a fluorescent molecule (e.g., a cyanine dye, e.g., Cy3, Cy 3.5, Cy5, Cy5.5, Cy7, or Cy7.5), a metal chelate, a contrast agent, a radionuclide, a positron emission tomography (PET) imaging agent, an infrared imaging agent, a near-IR imaging agent, a computer assisted tomography (CAT) imaging agent, a photon emission computerized tomography imaging agent (e.g., DIBO-DFO, where DFO chelates Zirconium-89), an X-ray imaging agent, or a magnetic resonance imaging (MRI) agent.

In an embodiment, a coupling reagent is a GMP grade material.

In some embodiments, the click reaction is a cycloaddition (e.g., a 1,3-dipolar cycloaddition or hetero-Diels-Alder cycloaddition), nucleophilic ring-opening (e.g., openings of strained heterocyclic electrophiles such as aziridines, epoxides, cyclic sulfates, aziridinium ions, and episulfonium ions), carbonyl chemistry of no-aldol type (e.g., formation of ureas, thioureas, hydrazones, oxime ethers, amides, or aromatic heterocycles), or an addition to a carbon-carbon multiple bond (e.g., epoxidation, aziridination, dihydroxylation, sulfenyl halide addition, nitosyl halide addition, or Michael addition). Examples of these types of click reaction are described in greater detail in Hein et al., Pharm. Res. 2008 October; 25(10):2216-2230, which is herein incorporated by reference in its entirety. In embodiments, the click reaction is a metal-free [3+2] cycloaddition reaction, Diels-Alder reaction, or thiol-alkene radical reaction. Examples of these types of click reaction are described in greater detail in Becer et al., Angew. Chem. Int. Ed. 2009, 48, 4900-4908, which is herein incorporated by reference in its entirety.

In an embodiment, the click signature is an alkyne/azide click signature (e.g., wherein the alkyne is a cyclooctyne, activated alkyne, or electron-deficient alkyne), e.g., the click signature comprises a triazole, e.g., a 1,2,3-triazole and/or a disubstituted triazole. In an embodiment, the click signature is a diene/dienophile click signature (e.g., wherein the dienophile comprises an alkene moiety), e.g., the click signature comprises a cycloalkene, e.g., a disubstituted alkene. In embodiments, the click signature is a tetrazine/alkene click signature, e.g., the click signature comprises a dihydropyrazine, e.g., a 1,2-dihydropyrazine. In embodiments, the click signature is a tetrazole/alkene click signature, e.g., the click signature comprises a diazole. In embodiments, the click signature is a dithioester/diene click signature, e.g., the click signature comprises a sulfur-containing ring, e.g., a tetrandrothiophene, e.g., a disubstituted tetrandrothiophene. In embodiments, the click signature is a dithioester/diene signature, e.g., the click signature comprises a sulfur-containing ring, e.g., a thiopyran. In embodiments, the click signature is a thiol/alkene click signature, e.g., the click signature comprises an alkyl sulfide.

In embodiments, the click reaction does not require a catalyst. In embodiments, the click reaction does not require copper ions, e.g., proceeds at substantially the same rate in the absence of copper ions as in the presence of copper ions, e.g., under conditions described in Tornoe, C. W. et al (2002). “Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides”. In embodiments, the click reaction proceeds efficiently at a temperature of about 10-40, 20-40, 20-30, 20-25, 30-40, or 35-40, or about 37 C. In embodiments, the click reaction proceeds efficiently at a temperature of below 50, 45, 40, 35, 30, 25, or 20 C.

In embodiments, the activation barrier for a click reaction is 24-30, 25-29, or 26-28 kcal/mol, e.g., about 27.8 kcal/mol or 26 kcal/mol. In embodiments, the activation barrier for a click reaction is the same as or no less than 50%, 40%, 30%, 20%, or 10%, different from the activation barrier of a Huisgen Cu-catalyzed cycloaddition reaction between an azide and a terminal alkene, e.g., as described in Hein et al. Click chemistry, a powerful tool for pharmaceutical sciences” Pharm Res. 2008 October; 25(10):2216-30.

In embodiments, the click reaction is exergonic, e.g., having a ΔG° of between −10 and −100, −20 and −90, −30 and −70, −40 and −70, −50 and −60, or about −61 kcal/mol. In embodiments, the ΔG° for a click reaction is the same as or no less than 50%, 40%, 30%, 20%, or 10%, different from the ΔG° of a Huisgen Cu-catalyzed cycloaddition reaction between an azide and a terminal alkene.

In embodiments, the click reaction has a ΔG° of between −30 and −140, −40 and −130, −50 and −120, −60 and −110, −70 and −100, −80 and −90, or about 84 kJ/mol.

One example of a cycloaddition reaction is the Huisgen 1,3-dipolar cycloaddition of a dipolarophile with a 1,3 dipolar component that produce five membered (hetero)cycles. Examples of dipolarophiles are alkenes, alkynes, and molecules that possess related heteroatom functional groups, such as carbonyls and nitriles. Specifically, another example is the 2+3 cycloaddition of alkyl azides and acetylenes. Other cycloaddition reactions include Diels-Alder reactions of a conjugated diene and a dienophile (such as an alkyne or alkene). Examples of cycloaddition reactions are described, e.g., in U.S. Pat. No. 9,517,291, which is herein incorporated by reference in its entirety.

Other examples of click reactions include a hydrosilation reaction of H—Si and simple non-activated vinyl compounds, urethane formation from alcohols and isocyanates, Menshutkin reactions of tertiary amines with alkyl iodides or alkyl trifluoromethanesulfonates, Michael additions, e.g., the very efficient maleimide-thiol reaction, atom transfer radical addition reactions between —SO₂Cl and an olefin (R¹, R²—C═C—R³, R⁴), metathesis, Staudinger reaction of phosphines with alkyl azides, oxidative coupling of thiols, nucleophilic substitution, especially of small strained rings like epoxy and aziridine compounds, carbonyl chemistry like formation of ureas, and addition reactions to carbon-carbon double bonds like dihydroxylation. Therefore, attached functionality may be chosen from acetylene bond, an azido-group, a nitrile group, acetylenic, amino group, phosphino group. The click chemistry reaction may result in the addition of a functional group selected from amino, primary amino, hydroxyl, sulfonate, benzotriazole, bromide, chloride, chloroformate, trimethylsilane, phosphonium bromide or bio-responsive functional group including polypeptides, proteins and nucleic acids.

Thus, suitable coupling reagents may comprise, for example, an amine, sulfate, thiol, hydroxyl, azide, alkyne, alkene, carboxyl groups aldehyde groups, sulfone groups, vinylsulfone groups, isocyanate groups, acid anhydride groups, epoxide groups, aziridine groups, episulfide groups, groups such as —CO₂N(COCH₂)₂, —CO₂N(COCH₂)₂, —CO₂H, —CHO, —CHOCH₂, —N.dbd.C.dbd.O, —SO₂CH.dbd.CH₂, —N(COCH)₂, —S—S—(C₅H₄N) and groups of the following structures wherein X is halogen and R is hydrogen or C₁ to C₄ alkyl:

In some embodiments, a click reaction forms very energy-efficient carbon-heteroatom bonds, in particular a ring opening nucleophilic reaction or a cycloaddition reaction. A type of reaction which is widely represented in click chemistry is the abovementioned alkyne-azide cycloaddition catalyzed with Cu(I). Examples of click reactions are also described, e.g., in U.S. Pat. No. 9,453,843, which is herein incorporated by reference in its entirety.

Click chemistry may generate substances quickly and reliably by joining small modular units together (see, e.g., Kolb et al. (2001) Angewandte Chemie Intl. Ed. 40:2004-2011; Evans (2007) Australian J. Chem. 60:384-395; Carlmark et al. (2009) Chem. Soc. Rev. 38:352-362; each herein incorporated by reference in its entirety). Examples of click chemistry are described, e.g., in U.S. Pat. No. 8,912,323, which is herein incorporated by reference in its entirety.

Agents, e.g., Exogenous Polypeptide Agents

The present invention features compositions of erythroid cells functionalized with an agent, and methods, preparations, and kits comprising the same. Exemplary agents for use in the invention are described herein.

In an embodiment, the agent is an agent described in WO2015/15302; or in WO2015/073587, each of which is hereby incorporated by reference in its entirety.

In an embodiment, the agent comprises a peptidic agent, e.g., a polypeptide, an enzyme, or an antibody.

In an embodiment, the agent comprises an exogenous polypeptide, e.g., a polypeptide that is not produced by a wild-type cell of that type or is present at a lower level in a wild-type cell than in a cell containing the exogenous polypeptide. In some embodiments, an exogenous polypeptide is a polypeptide conjugated to the surface of the cell by chemical or enzymatic means. In some embodiments, an exogenous polypeptide is a polypeptide encoded by a nucleic acid that was introduced into the cell, which nucleic acid is optionally not retained by the cell.

In an embodiment, the agent comprises a cytokine, a receptor, a ligand, a hormone, a growth factor, a blood factor, a lysosomal storage enzyme, asparaginase, or a fragment of any of the foregoing comprising an extracellular domain, counterligand binding domain, or other biologically active domain.

In an embodiment, the agent comprises an antigen, e.g., a tumor antigen, and infectious disease antigen, and autoantigen.

In an embodiment, the agent comprises a lipid, nucleic acid, e.g. RNA, DNA, siRNA, sugar, drug, or small molecule.

In an embodiment, the agent comprises a polypeptide of greater than about 30, 50, 75, 100, 150, 200, 250, 300, 350, or 400 kilodaltons.

In an embodiment, the agent, e.g., a polypeptide, comprises post translational modification, e.g., a post translational modification that is not made by erythroid cells, or made inefficiently by erythroid cells.

In an embodiment, the agent, e.g., a polypeptide, is toxic to, or compromises the growth, function, life span, or development of an erythroid cell.

In an embodiment, the agent comprises a multimeric polypeptide, e.g., a dimer, e.g., a homodimer or heterodimer, a trimer, e.g., a homotrimer or heterotrimer, or a tetramer, e.g., a homotetramer or heterotetramer, e.g., an antibody or a cell surface receptor, e.g., a receptor for a disease vector, e.g., a virus, a drug, or a toxin.

In an embodiment, the agent comprises a polypeptide, e.g., a multimeric polypeptide, comprising a plurality of cysteine bridges. In an embodiment, the agent comprises a polypeptide, e.g., a multimeric polypeptide, comprising one or more cysteine bridges.

In an embodiment, the agent comprises a difficult to express protein. For instance, in embodiments, the polypeptide agent has an amino acid sequence that, if expressed genetically in an erythroid cell, would reach a copy number of less than 1,000, 500, 200, or 100 copies of the protein per cell. In embodiments, the polypeptide agent has an amino acid sequence that, if expressed genetically in an erythroid cell, has inefficient translation or transcription, e.g., reaching a protein or mRNA level of less than 50%, 40%, 30%, 20%, 10%, 5%, 2%, 1% of a reference value, e.g., expression of a control protein such as ADA as described in WO2015/073587. In an embodiment, the polypeptide agent comprises an isoform, e.g., a splice variant, that if expressed genetically in an erythroid cell, would not be the most abundant isoform, e.g., would be present at a level at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90% lower than the level of the most abundant isoform.

In an embodiment, the agent comprises an antibody molecule, e.g., a polypeptide comprising one or more of the following: a) sufficient variable region to bind cognate antigen, e.g., HC CDR1, HC CDR2, and HC CDR3, LC CDR1, LC CDR2, and LC CDR3; b) a heavy chain constant sequence comprising one or more of CHL CH2, and CH3; c) a functional Fc region; and d) a modified or inactive Fc region, e.g., a mutationally inactivated Fc region or an Fc region having a glycosylation state that impairs Fc activity, e.g., a deglycosylated Fc region.

In an embodiment, the agent comprises an antibody, e.g., an IgA, IgG, IgG1, IgG2, IgM, IgE, or IgD.

In an embodiment, the agent comprises an anti-PDL1 antibody, an anti 4-1BB antibody, anti-α4β7 antibody, or protein A/G.

In some embodiments, the agent is deglycosylated. For instance, a glycosylated precursor may be treated with a deglycosylating enzyme (e.g., EndoS) to produce an agent.

In some embodiments, the agent comprises a polypeptide selected from or derived from one or more of the following classes, including but not limited to: an enzyme, a protease, a nuclease, a glycosidase, a lipase, a DNase, an antigen, an antibody-like molecule (e.g., a nanobody, an scFv, a duobody, or a multispecific antibody), a ligand of an antibody, a growth factor, a transporter, a cytokine, a chemokine, a growth factor receptor, a cytokine receptor, a chemokine receptor, an enzymatic recognition sequence, a transpeptidase recognition sequence, a protease recognition sequence, a cleavable domain, an intein, a DNA binding protein, an RNA binding protein, a complement regulatory molecule, a complement cascade molecule, a clotting cascade molecule, a chelator, a complement regulatory domain, an SCR domain, a CCP domain, an immunoglobulin or immunoglobulin-like domain, an armadillo repeat, a leucine zipper, a death effector domain, a cadherin repeat, an EF hand, a phosphotyrosine binding domain, a pleckstrin homology domain, an SCR homology 2 domain, a zinc finger domain, a cyclic peptide, a cell-penetrating peptide, a chaperone molecule, an integrin, a collagen, a carrier protein (e.g., albumin), a toxin binding peptide (e.g., a peptide that binds to a toxin from a bacterium, a parasite, a fungus or the environment), a myelination molecule, a prion protein binding molecule, a cluster of differentiation (CD) molecule, an immunomodulatory molecule (e.g., a co-stimulatory molecule, an activator of a co-stimulatory molecule, an inhibitor of a co-stimulatory molecule, a co-inhibitory molecule, an inhibitor of a co-inhibitory molecule or an activator of a co-inhibitory molecule), a cancer antigen or cancer cell marker, an antigen-presenting molecule, a pro-apoptotic molecule, a targeting moiety, an Fc receptor binding molecule, a tumor starvation enzyme, a DNA damage inhibitor, a cell-cycle inhibitor, a flexible linker, or an epitope tag. Specific examples of agents, e.g., polypeptides, are found, e.g., in WO2015/073587, WO2015/153102, and WO2016/183482, each of which is incorporated by reference in its entirety.

In some embodiments, the agent comprises one or more non-canonical amino acids. Non-canonical amino acids include, e.g., p-methoxyphenylalanine (pMpa); p-acetylphenylalanine (pApa); p-benzoylphenylalanine (pBpa); p-iodophenylalanine (pIpa); p-azidophenylalanine (pAzpa); p-propargyloxyphenylalanine (pPpa); α-aminocaprylic acid; o-nitrobenzylcysteine (o-NBC); 1,5-dansylalanine; and o-nitrobenzylserine (o-NBS), and other described in, e.g., U.S. Pat. No. 9,624,485, which is herein incorporated by reference in its entirety.

In some embodiments, the agent is other than a polypeptide. For instance, the agent can be a carbohydrate, small molecule, lipid, nucleic acid, therapeutic agent, naturally occurring or synthetic compound, or combinations thereof.

An exemplary exogenous polypeptide, e.g., a polypeptide agent of Table 1 or a variant thereof, includes:

a) a naturally occurring form of the polypeptide;

b) the polypeptide having a sequence appearing in a database, e.g., GenBank database, on Aug. 7, 2017;

c) a polypeptide having a sequence that differs by no more than 1, 2, 3, 4, 5 or 10 amino acid residues from a sequence of a) or b);

d) a polypeptide having a sequence that differs at no more than 1, 2, 3, 4, 5 or 10% its amino acids residues from a sequence of a) or b);

e) a polypeptide having a sequence that does not differ substantially from a sequence of a) orb); or

f) a polypeptide having a sequence of c), d), or e) that does not differ substantially in a biological activity, e.g., an enzymatic activity (e.g., specificity or turnover) or binding activity (e.g., binding specificity or affinity) from a protein having the sequence of a) or b).

In embodiments, the polypeptide comprises a polypeptide or fragment thereof, e.g., all or a fragment of a polypeptide of a), b), c), d), e), or f) of the preceding paragraph.

In embodiments, the agent comprises a polypeptide of Table 1, or an amino acid sequence having at least 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or 99.5% identity thereto, or a functional fragment thereof.

TABLE 1 Amino acid sequences of exemplary agents Agent Sequence 4-1BBL ACPWAVSGARASPGSAASPRLREGPELSPDDPAGLLDLRQGMFAQLVAQN VLLIDGPLSWYSDPGLAGVSLTGGLSYKEDTKELVVAKAGVYYVFFQLEL RRVVAGEGSGSVSLALHLQPLRSAAGAAALALTVDLPPASSEARNSAFGF QGRLLHLSAGQRLGVHLHTEARARHAWQLTQGATVLGLFRVTPEIPAGLP SPRSE (SEQ ID NO: 3) Anti-CD20 Rituximab heavy chain chimeric: QVQLQQPGAELVKPGASVKMSCKASGYTFTSYNMHWVKQTPGRGLEWIGA IYPGNGDTSYNQKFKGKATLTADKSSSTAYMQLSSLTSEDSAVYYCARST YYGGDWYFNVWGAGTTVTVSAASTKGPSVFPLAPSSKSTSGGTAALGCLV KDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQ TYICNVNHKPSNTKVDKKAEPKSCDKTHTCPPCPAPELLGGPSVFLFPPK PKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQY NSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREP QVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPP VLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPG K (SEQ ID NO: 4) Rituximab light chain chimeric: QIVLSQSPAILSASPGEKVTMTCRASSSVSYIHWFQQKPGSSPKPWIYAT SNLASGVPVRFSGSGSGTSYSLTISRVEAEDAATYYCQQWTSNPPTFGGG TKLEIKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVD NALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGL SSPVTKSFNRGEC (SEQ ID NO: 5) TRAIL Soluble TRAIL variant DR4-1 MAMMEVQGGPSLGQTCVLIVIFTVLLQSLCVAVTYVYFTNELKQMQDKYS KSGIACFLKEDDSYWDPNDEESMNSPCWQVKWQLRQLVRKMILRTSEETI STVQEKQQNISPLVRERGPQRVAAHITGTRRRSNTLSSPNSKNEKALGRK INSWESSRSGHSFLSNLHLRNGELVIHEKGFYYIYSQTYFRFQEEIKENT KNDKQMVQYIYKYTSYPDPILLMKSARNSCWSKDAEYGLYSIYQGGIFEL KENDRIFVSVTNEHLIDMDHEASFFGAFLVG (SEQ ID NO: 6) Soluble TRAIL variant DR4-2 MAMMEVQGGPSLGQTCVLIVIFTVLLQSLCVAVTYVYFTNELKQMQDKYS KSGIACFLKEDDSYWDPNDEESMNSPCWQVKWQLRQLVRKMILRTSEETI STVQEKQQNISPLVRERGPQRVAAHITGTRGRSNTLSSPNSKNEKALGRK INSWESSRRGHSFLSNLHLRNGELVIHEKGFYYIYSQTYFRFQEEIKENT KNDKQMVQYIYKYTSYPDPILLMKSARNSCWSKDAEYGLYSIYQGGIFEL KENDRIFVSVTNEHLIDMDHEASFFGAFLVG (SEQ ID NO: 7) Soluble TRAIL variant DR4-3 MAMMEVQGGPSLGQTCVLIVIFTVLLQSLCVAVTYVYFTNELKQMQDKYS KSGIACFLKEDDSYWDPNDEESMNSPCWQVKWQLRQLVRKMILRTSEETI STVQEKQQNISPLVRERGPQRVAAHITGTRRRSNTLSSPNSKNEKALGIK INSWESSRRGHSFLSNLHLRNGELVIHEKGFYYIYSQTYFRFQEEIKENT KNDKQMVQYIYKYTDYPDPILLMKSARNSCWSKDAEYGLYSIYQGGIFEL KENDRIFVSVTNEHLIDMDHEASFFGAFLVG (SEQ ID NO: 8) Soluble TRAIL variant DR5-1 MAMMEVQGGPSLGQTCVLIVIFTVLLQSLCVAVTYVYFTNELKQMQDKYS KSGIACFLKEDDSYWDPNDEESMNSPCWQVKWQLRQLVRKMILRTSEETI STVQEKQQNISPLVRERGPQRVAAHITGTRGRSNTLSSPNSKNEKALGRK INSWESSRSGHSFLSNLHLRNGELVIHEKGFYYIYSQTYFRFQEEIKENT KNDKQMVQYIYKYTSYPDPILLMKSARNSCWSKDAEYGLYSIYQGGIFEL KENDRIFVSVTNEHLIDMHHEASFFGAFLVG (SEQ ID NO: 9) Soluble TRAIL variant DR5-2 MAMMEVQGGPSLGQTCVLIVIFTVLLQSLCVAVTYVYFTNELKQMQDKYS KSGIACFLKEDDSYWDPNDEESMNSPCWQVKWQLRQLVRKMILRTSEETI STVQEKQQNISPLVRERGPQRVAAHITGTRGRSNTLSSPNSKNEKALGRK INSWESSRSGHSFLSNLHLRNGELVIHEKGFYYIYSQTYFRFQERIKENT KNDKQMVQYIYKYTSYPDPILLMKSARNSCWSKDAEYGLYSIYQGGIFEL KENDRIFVSVTNEHLIDMHHEASFFGAFLVG (SEQ ID NO: 10) Anti-PD-L1 VQLVESGGGLVQPGGSLRLSCAASGFTFSDSWIHWVRQAPGKGLEWVAWI scFv SPYGGSTYYADSVKGRFTISADTSKNTAYLQMNSLRAEDTAVYYCARRHW PGGFDYWGQGTLVTVSSGGGGSGGGGSGGGGSIQMTQSPSSLSASVGDRV TITCRASQDVSTAVAWYQQKPGKAPKLLIYSASFLYSGVPSRFSGSGSGT DFTLTISSLQPEDFATYYCQQYLYHPATFGQGTKVEIK (SEQ ID NO: 11) PAL MKTLSQAQSKTSSQQFSFTGNSSANVIIGNQKLTINDVARVARNGTLVSL TNNTDILQGIQASCDYINNAVESGEPIYGVTSGFGGMANVAISREQASEL QTNLVWFLKTGAGNKLPLADVRAAMLLRANSHMRGASGIRLELIKRMEIF LNAGVTPYVYEFGSIGASGDLVPLSYITGSLIGLDPSFKVDFNGKEMDAP TALRQLNLSPLTLLPKEGLAMMNGTSVMTGIAANCVYDTQILTAIAMGVH ALDIQALNGTNQSFHPFIHNSKPHPGQLWAADQMISLLANSQLVRDELDG KHDYRDHELIQDRYSLRCLPQYLGPIVDGISQIAKQIEIEINSVTDNPLI DVDNQASYHGGNFLGQYVGMGMDHLRYYIGLLAKHLDVQIALLASPEFSN GLPPSLLGNRERKVNMGLKGLQICGNSIMPLLTFYGNSIADREPTHAEQF NQNINSQGYTSATLARRSVDIFQNYVAIALMFGVQAVDLRTYKKTGHYDA RACLSPATERLYSAVRHVVGQKPTSDRPYIWNDNEQGLDEHIARISADIA AGGVIVQAVQDILPCLH (SEQ ID NO: 12) Y vb MADKLPNIVILATGGTIAGSAATGTQTTGYKAGALGVDTLINAVPEVKKL Asparaginase ANVKGEQFSNMASENIVITGDVVLKLSQRVNELLARDDVDGVVITHGTDT VEESAYELHLTVKSDKPVVFVAAMRPATAISADGPMNLLEAVRVAGDKQS RGRGVMVVLNDRIGSARYITKTNASTLDTFKANEEGYLGVIIGNRIYYQN RIDKLHTTRSVFDVRGLTSLPKVDILYGYQDDPEYLYDAAIQHGVKGIVY AGMGAGSVSVRGIAGMRKAMEKGVVVIRSTRTGNGIVPPDEELPGLVSDS LNPAHARILLMLALTRTSDPKVIQEYFHTY (SEQ ID NO: 13) Anti-a4b7 Heavy chain variable region: QVQLVQSGAEVKKPGASVKVSCKGSGYTFTSYWMIHWVRQAPGQRLEWIG EIDPSESNTNYNQKFKGRVTLTVDISASTAYMELSSLRSEDTAVYYCARG GYDGWDYAIDYWGQGTLVTVSS (SEQ ID NO: 14) Light chain variable region: DVVMTQSPLSLPVTPGEPASISCRSSQSLAKSYGNTYLSWYLQKPGQSPQ LLIYGISNRFSGVPDRFSGSGSGTDFTLKISRVEAEDVGVYYCLQGTHQP YTFGQGTKVEIK (SEQ ID NO: 15) Human IL10 SPGQGTQSENSCTHFPGNLPNMLRDLRDAFSRVKTFFQMKDQLDNLLLKE SLLEDFKGYLGCQALSEMIQFYLEEVMPQAENQDPDIKAHVNSLGENLKT LRLRLRRCHRELPCENKSKAVEQVKNAENKLQEKGIYKAMSEEDIFINYI EAYMTMKIRN (SEQ ID NO: 16) Clotting ANSFLEEMKKGHLERECMEETCSYEEAREVFEDSDKTNEFWNKYKDGDQC Factor X ETSPCQNQGKCKDGLGEYTCTCLEGFEGKNCELFTRKLCSLDNGDCDQFC HEEQNSVVCSCARGYTLADNGKACIPTGPYPCGKQTLERRKRSVAQATSS SGEAPDSITWKPYDAADLDPTENPFDLLDFNQTQPERGDNNLTRIVGGQE CKDGECPWQALLINEENEGFCGGTILSEFYILTAAHCLYQAKREKVRVGD RNTEQEEGGEAVHEVEVVIKHNRFTKETYDEDIAVLRLKTPITERWINVA PACLPERDWAESTLMTQKTGIVSGEGRTHEKGRQSTRLKMLEVPYVDRNS CKLSSSFIITQNMFCAGYDTKQEDACQGDSGGPHVTRFKDTYEVTGIVSW GEGCARKGKYGIYTKVTAFLKWIDRSMKTRGLPKAKSHAPEVITSSPLK (SEQ ID NO: 17)

In some embodiments, an exogenous polypeptide described herein is at least 200, 300, 400, 500, 600, 700, or 800 amino acids in length. In some embodiments, the exogenous polypeptide is between 200-300, 300-400, 400-500, 500-600, 600-700, or 700-800 amino acids in length.

In some embodiments, an erythroid cell, e.g., an enucleated erythroid cell, comprises at least 1,000, 5,000, 10,000, 15,000, 20,000, 25,000, 30,000, 50,000, 100,000, 200,000, or 500,000 copies of an exogenous polypeptide described herein, e.g., of Table 1.

In embodiments, the agent comprises one or more post-translational modifications. Post-translation modifications include cleavage (e.g., proteolytic cleavage), cyclization, glycosylation, phosphorylation, conjugation to a hydrophobic group (e.g., myristoylation, palmitoylation, isoprenylation, prenylation, or glypiation), conjugation to a cofactor (e.g., lipoylation, flavin moiety (e.g., FMN or FAD), heme C attachment, phosphopantetheinylation, or retinylidene Schiff base formation), diphthamide formation, ethanolamine phosphoglycerol attachment, hypusine formation, acylation (e.g. O-acylation, N-acylation, or S-acylation), formylation, acetylation, alkylation (e.g., methylation or ethylation), amidation, butyrylation, gamma-carboxylation, malonylation, hydroxylation, iodination, nucleotide addition such as ADP-ribosylation, oxidation, phosphate ester (O-linked) or phosphoramidate (N-linked) formation, (e.g., phosphorylation or adenylylation), propionylation, pyroglutamate formation, S-glutathionylation, S-nitrosylation, succinylation, sulfation, ISGylation, SUMOylation, ubiquitination, Neddylation, or a chemical modification of an amino acid (e.g., citrullination, deamidation, eliminylation, or carbamylation), formation of a disulfide bridge, racemization (e.g., of proline, serine, alanine, or methionine), or any combination thereof. In embodiments, glycosylation includes the addition of a glycosyl group to arginine, asparagine, cysteine, hydroxylysine, serine, threonine, tyrosine, or tryptophan, resulting in a glycoprotein. In embodiments, the glycosylation comprises, e.g., O-linked glycosylation or N-linked glycosylation.

In embodiments, the cell comprises a plurality of agents, e.g., at least 10, 20, 50, 100, 200, 500, or 1,000 different agents. In some embodiments, the plurality of agents comprise a plurality of vaccine antigens. In some embodiments, the plurality of agents have sequence similarity to each other but vary between each other at at least 1, 2, 5, 10, 20, 50, or 100 amino acid positions. In some embodiments, each agent in the plurality has at least 70%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% identity to each other agent in the plurality. In some embodiments, each agent in the plurality has at least 70%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% identity to at least 1, 2, 5, 10, 20, 50, or 100 other agents in the plurality.

Geometry of Coupling Reagents on Agents

A coupling agent can be attached a variety of different positions on an agent. A coupling agent can comprise a substrate reactive moiety suitable, e.g., for binding (e.g., covalently) to a substrate such as an agent (e.g., polypeptide). A coupling agent can further comprise a coupling moiety, e.g., a click coupling moiety suitable, e.g., for binding (e.g., covalently) to a second coupling agent. A suitable substrate reactive moiety can be chosen to direct the attachment of the coupling agent with the agent (e.g., polypeptide).

For instance, in some embodiments, the substrate reaction moiety is capable of reacting with an NH₂ group, e.g., on a side chain of lysine or the N terminus of the agent. An example of a substrate reaction moiety capable of reacting with an NH₂ group is an NHS ester, Imidoester, Pentafluorophenyl ester, or Hydroxymethyl phosphine. In some embodiments, the substrate reaction moiety is capable of reacting with a carboxyl of the agent, e.g., on a side chain of aspartic acid or glutamic acid or the C-terminus of the agent. An example of a substrate reaction moiety capable of reacting with a carboxyl is a carbodiimide. In some embodiments, the substrate reaction moiety is capable of reacting with a sulfhydryl of the agent, e.g., on a side chain of cysteine. An example of a substrate reaction moiety capable of reacting with a sulfhydryl is Maleimide, Haloacetyl (e.g., Bromo- or Iodo-), Pyridyldisulfide, Thiosulfonate, or Vinylsulfone. An agent having a disulfide bridge may be placed under reducing conditions to convert the disulfide bridge to sulfhydryls. In some embodiments, the substrate reaction moiety is capable of reacting with a carbonyl of the agent. For instance, a ketone or aldehyde group can be created in glycoproteins, e.g., by oxidizing the polysaccharide post-translational modifications, for instance with sodium meta-periodate. An example of a substrate reaction moiety capable of reacting with a carbonyl is a hydrazide or alkoxyamine.

A moiety on an agent can be linked to a preselected moiety on a cell. For instance, in some embodiments, an NH₂ group on the agent is linked to an NH₂ group, carboxyl, sulfhydryl, or carbonyl of the cell. In embodiments, a carboxyl group on the agent is linked to an NH₂ group, carboxyl, sulfhydryl, or carbonyl of the cell. In embodiments, a sulfhydryl group on the agent is linked to an NH₂ group, carboxyl, sulfhydryl, or carbonyl of the cell. In embodiments, a carbonyl group on the agent is linked to an NH₂ group, carboxyl, sulfhydryl, or carbonyl of the cell.

Clickable Format Agents

In some embodiments, the agent is a polypeptide with a coupling agent linked to a predetermined amino acid. Briefly, the polypeptide agent can be produced in a first cell (a “factory cell”, such that a non-canonical amino acid (ncAA) comprising a first coupling reagent is present at one or more amino acid positions of the polypeptide agent. The agent can then be coupled to a second cell that has a second coupling reagent at the cell surface, thereby coupling the polypeptide agent to the second cell. This technology can use site-specific incorporation of the ncAA, such that the orientation of the agent on the cell surface is controlled.

For instance, ncAAs can be introduced into the polypeptide agent by genetically incorporating an Amber stop codon (TAG) at the site of interest in a nucleic acid encoding the polypeptide agent, e.g., as described in Nikic et al. Nature Protocols 2015 which is herein incorporated by reference in its entirety. The amber stop codon can be incorporated, e.g., at the N-terminus, C-terminus, or interior of the protein. This plasmid encoding the polypeptide agent can be co-transfected into a factory cell (e.g., HEK293 or CHO cell) with another plasmid encoding an aminoacyl-tRNA synthase/tRNA pair that is orthogonal to the host's translational machinery. In the presence of ncAA, there is read through of the Amber codon and incorporation of the ncAA. For instance, one may use M. mazei pyrrolysine aminoacyl-tRNA synthetase/tRNA (PylRS/tRNAPyl) with Y306A and Y384F mutations and the ncAAs: cyclooctyne-lysine (SCO), Endo Bicyclo [6.1.0] nonyne-lysine (endoBCN), Exo Bicyclo [6.1.0] nonyne-lysine (exoBCN), or Rac Bicyclo [6.1.0] nonyne-lysine (racBCN). Other suitable ncAAs are described in the section herein entitled “Clickable format cells”. The plasmid may further encode a sequence that directs secretion of the protein. Transient transfection or a stable cell line can be used.

Once the clickable format protein is produced, it can be reacted with a cell having a second coupling agent. For instance, the cell can by an erythroid cell having a click linker, e.g., a click linker comprising an azide.

Geometry of Coupling Reagents on Cells

A coupling agent can be attached a variety of different positions on a cell. A coupling agent can comprise a substrate reactive moiety suitable, e.g., for binding (e.g., covalently) to a substrate such as a cell (e.g., a polypeptide or carbohydrate moiety on the cell). A coupling agent can further comprise a coupling moiety, e.g., a click coupling moiety suitable, e.g., for binding (e.g., covalently) to a second coupling agent. A suitable substrate reactive moiety can be chosen to direct the attachment of the coupling agent with the cell.

Suitable substrate reaction moieties are described herein, e.g., in the section entitled “Geometry of coupling reagents on agents.”

A moiety on a cell can be linked to a preselected moiety on an agent. For instance, in some embodiments, an NH₂ group on the cell is linked to an NH₂ group, carboxyl, sulfhydryl, or carbonyl of the agent. In embodiments, a carboxyl group on the cell is linked to an NH₂ group, carboxyl, sulfhydryl, or carbonyl of the agent. In embodiments, a sulfhydryl group on the cell is linked to an NH₂ group, carboxyl, sulfhydryl, or carbonyl of the agent. In embodiments, a carbonyl group on the cell is linked to an NH₂ group, carboxyl, sulfhydryl, or carbonyl of the agent.

Sortase and Click

In some embodiments, a transpeptidase reaction such as a sortase reaction is used to attach a linker to an agent or to a cell.

For instance, in some embodiments a polypeptide agent comprises a transpeptidase recognition sequence, e.g., a sortase recognition sequence. The polypeptide agent may be contacted with a sortase and a coupling reagent that has a compatible sortase recognition sequence, thereby sortagging the coupling reagent onto the polypeptide agent. The polypeptide agent can then be reacted with a cell having a second coupling agent. The second coupling agent may be, e.g., on an NH₂ group, carboxyl, sulfhydryl, or carbonyl of the cell.

In some embodiments a cell (e.g., a polypeptide or carbohydrate on the cell) comprises a transpeptidase recognition sequence, e.g., a sortase recognition sequence. For instance, the cell may genetically express a transmembrane protein comprising a sortase recognition sequence at the cell surface. The cell may be contacted with a sortase and a coupling reagent that has a compatible sortase recognition sequence, thereby sortagging the coupling reagent onto the cell.

The cell can then be reacted with a polypeptide agent having a second coupling agent. The second coupling agent may be, e.g., on an NH₂ group, carboxyl, sulfhydryl, or carbonyl of the polypeptide agent.

In some embodiments, the polypeptide agent does not comprise a transpeptidase recognition sequence, e.g., a sortase recognition sequence. In embodiments, the cell does not comprise an exogenous transpeptidase recognition sequence, e.g., a sortase recognition sequence. In embodiments, the method does not comprise a sortagging step. In embodiments, the functionalized erythroid cell does not comprise a sortase transfer signature.

A sortase can enzymatically conjugate two sortase recognition motifs together. The first sortase recognition motif can be a sortase donor motif and the second sortase recognition motif can be a sortase acceptor motif.

Sortase recognition motifs include LPXTA (SEQ ID NO: 18) and LPXTG (SEQ ID NO: 1), in which X is any amino acid residue. One exemplary sortase recognition motif is LPXTG (SEQ ID NO: 1), in which X can be any amino acid residue (naturally-occurring or non-canonical), e.g., any of the 20 standard amino acids found most commonly in proteins found in living organisms. In some examples, the recognition motif is LPXTG (SEQ ID NO: 19) or LPXT, in which X is D, E, A, N, Q, K, or R. In other examples, X is selected from K, E, N, Q, or A in an LPXTG (SEQ ID NO: 20) or LPXT motif, which are recognizable by a sortase A. In yet other examples, X is selected from K, S, E, L, A, or N in an LPXTG (SEQ ID NO: 21) or LPXT motif, which are recognizable by a class C sortase. Exemplary sortase recognition motifs include, but are not limited to, LPKTG (SEQ ID NO: 22), LPITG (SEQ ID NO: 23), LPDTA (SEQ ID NO: 24), SPKTG (SEQ ID NO: 25), LAETG (SEQ ID NO: 26), LAATG (SEQ ID NO: 27), LAHTG (SEQ ID NO: 28), LASTG (SEQ ID NO: 29), LPLTG (SEQ ID NO: 30), LSRTG (SEQ ID NO: 31), LPETG (SEQ ID NO: 32), VPDTG (SEQ ID NO: 33), IPQTG (SEQ ID NO: 34), YPRRG (SEQ ID NO: 35), LPMTG (SEQ ID NO: 36), LAFTG (SEQ ID NO: 37), LPQTS (SEQ ID NO: 38), LPXT, LAXT, LPXA, LGXT, IPXT, NPXT, NPQS (SEQ ID NO: 39), LPST (SEQ ID NO: 40), NSKT (SEQ ID NO: 41), NPQT (SEQ ID NO: 42), NAKT (SEQ ID NO: 43), LPIT (SEQ ID NO: 44), LAET (SEQ ID NO: 45), LPXAG (SEQ ID NO: 46), LPNAG (SEQ ID NO: 47), LPXTA (SEQ ID NO: 18), LPNTA (SEQ ID NO: 48), LGXTG (SEQ ID NO: 49), LGATG (SEQ ID NO: 50), IPXTG (SEQ ID NO: 51), IPNTG (SEQ ID NO: 52), IPETG (SEQ ID NO: 53), NPXTX, NP[Q/K]-[T/s]-[N/G/s], NPQTN (SEQ ID NO: 54), NPKTG (SEQ ID NO: 55), NSKTA (SEQ ID NO: 56), NPQTG (SEQ ID NO: 57), NAKTN (SEQ ID NO: 58), NPQSS (SEQ ID NO: 59), NA-[E/A/S/H]-TG (SEQ ID NO: 60), LAXTG (SEQ ID NO: 61), QVPTGV (SEQ ID NO: 62), LPXTX, LP[Q/K]T[A/S]T (SEQ ID NO: 63), or LPXT[A/S].

Sortase acceptor motifs include oligoglycines or oligoalanines, such as a 1-5 glycine fragment or a 1-5 alanine fragment. In some examples, the oligoglycine consists of 3 or 5 glycine residues. In other examples, the oligoalanine consists of 3 or 5 alanine residues.

A sortase transfer signature can be created by a sortase reaction. For instance, a sortase-mediated reaction of LPXTGG (SEQ ID NO: 2) with (G)_(n) can produce a sortase transfer signature of LPXT(G)_(n) (SEQ ID NO: 1). In embodiments, the sortase transfer signature comprises a sequence of a sortase recognition motif described herein, e.g., in this section. In embodiments, the sortase transfer signature further comprises one or more alanine or glycine amino acids, e.g., at the C-terminus of the sequence of the sortase recognition motif.

A variety of sortases are described, e.g., in WO2014/183071 (e.g., on pages 33-37 therein), which application is herein incorporated by reference in its entirety.

Second Agents Added by Various Methods

In some embodiments, a cell (e.g., enucleated erythroid cell) described herein comprises (in addition to its first agent) a second agent, e.g, an exogenous polypeptide agent. In some embodiments, the second agent is conjugated to the cell, e.g., using click chemistry. In some embodiments, the second agent comprises a protein expressed from an exogenous nucleic acid (e.g., DNA or RNA) introduced into the cell or a precursor thereof. In some embodiments, the second agent comprises a protein sortagged onto the cell. In some embodiments, the second agent is hypotonically loaded into the cell. In some embodiments, the second agent is not covalently linked to a click signature or a residual linker.

Non-Conjugation Methods of Adding an Agent to a Cell

While in many embodiments an agent is conjugated to a cell, e.g., using click chemistry, it is understood that any agent described herein may also be added to a cell using a variety of methods. Accordingly, in some aspects, the present disclosure provides a cell (e.g., an erythroid cell, e.g., an enucleated erythroid cell) comprising an agent, e.g., exogenous polypeptide agent, described herein, e.g., a polypeptide of Table 1, or a fragment or variant thereof. The cell can be made, e.g., by introducing a nucleic acid encoding the protein into the cell or a precursor thereof, by sortagging, by hypotonic loading, or by chemical conjugation.

Methods of Treatment with Compositions Herein, e.g., Erythroid Cells

Methods of administering engineered erythroid cells are described, e.g., in WO2015/153102 and WO2015/073587, each of which is incorporated by reference in its entirety.

In embodiments, the erythroid cells described herein are administered to a subject, e.g., a mammal, e.g., a human. Exemplary mammals that can be treated include without limitation, humans, domestic animals (e.g., dogs, cats and the like), farm animals (e.g., cows, sheep, pigs, horses and the like) and laboratory animals (e.g., monkey, rats, mice, rabbits, guinea pigs and the like). The methods described herein are applicable to both human therapy and veterinary applications.

In some embodiments, the erythroid cells described herein are administered to a subject for the treatment or prevention of inflammation and diseases associated with inflammation, including sepsis, autoimmune disease, cancer, and microbial infections. In some embodiments, the erythroid cells described herein are administered to a subject with an autoimmune disease, e.g., multiple sclerosis, type 1 diabetes, rheumatoid arthritis, membranous nephritis, or any of the diseases listed in Table F of WO2015/153102, which is incorporated by reference herein in its entirety.

In some aspects, the present disclosure provides a method of treating a disease or condition described herein, comprising administering to a subject in need thereof a composition described herein, e.g., an erythroid cell described herein. In some embodiments, the disease or condition is a cancer, e.g., a cancer described herein. In some aspects, the disclosure provides a use of an erythroid cell described herein for treating a disease or condition described herein, e.g., a cancer. In some aspects, the disclosure provides a use of an erythroid cell described herein for manufacture of a medicament for treating a disease or condition described herein, e.g., a cancer. Exemplary cancers are described in WO2015/073587, which is incorporated by reference herein in its entirety.

In some embodiments, the erythroid cells are administered intravenously, e.g., by intravenous infusion.

All references cited herein are incorporated herein by reference in their entirety.

EXAMPLES

In order that the invention described herein may be more fully understood, the following examples are set forth. The examples described in this application are offered to illustrate the compositions, preparations, and methods provided herein and are not to be construed in any way as limiting their scope.

Example 1: Preparation of an Erythroid Cell Comprising a Click Handle

A population of erythroid cells was prepared for labeling with a coupling reagent. Erythrocytes obtained from whole blood were filtered and concentrated to a density of 3.31×10⁹ cells/mL. The cells were washed twice with ice-cold phosphate-buffered saline (PBS, 2×1 mL) and the residual volume was removed by pipette. PBS at pH 8 (100 uL) was then added to the cells.

Stock solutions of the following coupling reagents were prepared at 1 mM (DBCO-sulfo-NHS ester, DBCO-PEG5-NHS ester, 3-azidopropionic acid sulfo-NHS ester, and azido-PEG4-NHS ester), and each solution was added to a sample of cells for a final coupling reagent concentration of either 0.1 mM or 0.04 mM. The reaction was incubated at room temperature for 30 minutes, with gentle agitation every 10 minutes.

The labeling reaction was quenched by adding 1 mL PBSA (PBS with 0.1% BSA) to each reaction, and allowing each reaction to incubate for 5 minutes at room temperature. The cells were pelleted by centrifugation (5 minutes at 2500 rpm), and the supernatant was removed by aspiration. The cell pellet was then washed with PBS (1 mL) and pelleted again (5 minutes at 2500 rpm), and the supernatant was removed by aspiration.

In order to detect the level of labeling, a detection reagent stock solution comprising either Cy5-biotin-azide or Cy5-DBCO was prepared at 100 nM. The detection reagent (100 uL) was added to each reaction, and the reactions were incubated at room temperature for 30 minutes. The labeling efficiency was determined by flow cytometry, and is summarized below in Table 2.

TABLE 2 Conjugation efficiency of click reactions Sample Conjugation # Click chemistry reagent Detection reagent Efficiency (%) 1 DBCO-Sulfo-NHS ester 0.1 mM Cy5 biotin Azide 88.5 2 DBCO-Sulfo-NHS ester 0.04 mM Cy5 biotin Azide 38.3 3 Sulfo-DBCO-NHS ester 0.1 mM Cy5 Azide 74.4 4 Sulfo-DBCO-NHS ester 0.04 mM Cy5 Azide 55.1 5 DBCO-PEG4-NHS ester 0.1 mM Cy5 Azide 97.4 6 DBCO-PEG4-NHS ester 0.04 mM Cy5 Azide 96.1 7 DBCO-PEG5-NHS ester 0.1 mM Cy5 biotin Azide 83.1 8 DBCO-PEG5-NHS ester 0.04 mM Cy5 biotin Azide 29.7 9 DBCO-PEG13-NHS ester 0.1 mM Cy5 Azide 98.0 10 DBCO-PEG13-NHS ester 0.04 mM Cy5 Azide 95.5 11 3-Azidopropionic Acid Sulfo-NHS Cy5 DBCO 99.8 ester 0.1 mM 12 3-Azidopropionic Acid Sulfo-NHS Cy5 DBCO 97.9 ester 0.04 mM 13 6-Azidohexanoic Acid Sulfo-NHS Cy5 DBCO 98.9 ester 0.1 mM 14 6-Azidohexanoic Acid Sulfo-NHS Cy5 DBCO 99.3 ester 0.04 mM 15 Azido-PEG4-NHS ester 0.1 mM Cy5 DBCO 99.1 16 Azido-PEG4-NHS ester 0.04 mM Cy5 DBCO 67.0 17 TCO-PEG4-NHS ester 0.1 mM Cy5 Methyltetrazine 1.4 18 TCO-PEG4-NHS ester 0.04 mM Cy5 Methyltetrazine 3.0 19 TCO-PEG12-NHS ester 0.1 mM Cy5 Methyltetrazine 96.7 20 TCO-PEG12-NHS ester 0.04 mM Cy5 Methyltetrazine 80.5 21 Methyltetrazine-Sulfo-NHS ester Cy5-TCO 97.6  0.1 mM 22 Methyltetrazine-Sulfo-NHS ester Cy5-TCO 95.1 0.04 mM 23 Methyltetrazine-PEG4-NHS ester Cy5-TCO 97.5  0.1 mM 24 Methyltetrazine-PEG4-NHS ester Cy5-TCO 98.7 0.04 mM 25 Control (N/A) Cy5 biotin Azide 0.74 26 Control (N/A) Cy5 DBCO 0.43

Example 2: Preparation of an Agent Comprising a Click Handle

Proteins of interest were prepared for coupling to erythroid cells by labeling with a coupling reagent. Exemplary proteins for labeling included antibodies (e.g., an anti-PDL1 (rat anti-mouse PDL1 antibody) and anti-α4β7 (a rat anti-mouse a4β7 antibody)), 4-1BB ligand, and protein A/G. Proteins were typically desalted, buffer exchanged to PBS, and concentrated to ≥1 mg/mL prior to labeling, and the pH was adjusted to pH 7-8. Antibodies were routinely deglycosylated with an endoglycosidase (e.g., EndoS) to prevent ADCC; the endoglycosidase was removed using an affinity purification prior to addition of the coupling reagent.

Stock solutions of coupling reagents were prepared as described in Example 1. For protein solutions with a concentration greater than 5 mg/mL, the coupling reagent was added at a 10-fold molar excess relative to the protein concentration. For protein solutions with a concentration less than 5 mg/mL, the coupling reagent was added at a 20-fold to 50-fold molar excess relative to the protein concentration. The protein labeling reaction was incubated at room temperature for 30 minutes, with gentle agitation every 10 minutes.

In order to detect the level of labeling, a detection reagent stock solution comprising either Cy5-biotin-azide or WS-DBCO-biotin was prepared and added to each reaction, and the reactions were incubated at room temperature for 30 minutes. The labeling efficiency was determined by Western blotting, using an anti-biotin antibody for detection.

In an alternative method of detection for degree of labeling, the Nanodrop UV-Vis program was used to read approximately 1-3 μL of labeled protein at absorbance 280 nm and 309 nm with a baseline correction at 750 nm.

Example 3: Production of Enucleated Erythroid Cells Comprising an Agent Covalently Linked to the Cell Surface by a Residual Linker Comprising a Click Signature

Proteins were coupled to erythroid cells according the general procedure described below. Erythroid cells labeled with 3-azidopropionic acid sulfo-NHS ester (Sample #11 in Table 2) as described in Example 1 were incubated with 1.5-3 molar equivalents of an anti-α4β7 (mouse) antibody labeled with DBCO-sulfo-NHS ester or DBCO-PEG5-NHS ester, and the reaction was incubated at room temperature for up to 12 hours at either room temperature or 4° C. The cells were then washed with PBS or PBSA, and stained with an anti-mouse antibody linked to a detection agent. The cells were then analyzed via flow cytometry to determine the protein labeling efficiency. As shown in FIGS. 2A-2C, the protein labeling efficiency was determined to be 98.4% for the DBCO-sulfo-NHS ester-linked anti-α4β7 antibody (FIG. 2B) and 94.4% for the DBCO-PEG5-NHS ester-linked anti-α4β7 antibody (FIG. 2C).

In another experiment, proteins were coupled to erythroid cells in small reaction volumes using high concentrations of protein. To perform the reaction, erythroid cells were labeled with 3-Azidopropionic acid Sulfo-NHS Ester (AS). An anti-α4β7 (rat) antibody was labeled with DBCO-sulfo-NHS ester (DS) or DBCO-PEG5-NHS ester (DP). The labeled cells were incubated with 1-20E6 molar equivalents per cell of the anti-α4β7 antibody in an undiluted in a volume of 5-10 μL, for 1 hour at 23° C. The cells were then washed with phosphate buffered saline with 0.1% bovine serum albumin, and stained with an anti-rat antibody linked to a fluorophore (fluorescein isothiocyanate). The cells were then analyzed via flow cytometry to determine the protein clicking efficiency. As shown in Table 3, the protein clicking efficiency was determined to be in the range of 98.9-99.8%. A cell is considered positive for fluorescence if its fluorescence is greater than 99% of otherwise similar unlabeled cells. This experiment indicates that it is possible to label a very high percentage of the cells with a protein, e.g., by using a small reaction volume and high amount of protein. This experiment also indicates it is possible to link a multimer to the cell, as the antibody has two heavy chains and two light chains. This Example also indicates it is possible to link large moieties to a cell, as the antibody has a molecular weight of about 150 kDa.

TABLE 3 Efficiency of labeling cells with anti-α4β7 Volume molar Number of of excess Percent cells AS-labeled Concentration click DBCO: DBCO positive for cells of AS reaction protein reagent fluorescence 1E7 0.1 mM  5 ul 10 DS 99.8% 1E7 0.1 mM 10 ul 10 DP 98.9% 1E7 0.1 mM 10 ul 50 DS 99.6% 1E8 0.1 mM 10 ul 10 DP 99.7% 1E8 0.1 mM 10 ul 50 DS 99.7%

Example 4: Coupling of an Antibody Agent to Erythroid Cells Via a Residual Linker Comprising a Click Signature

It is sometimes desirable to conjugate a protein having multiple subunits and/or post-translational modifications to a cell. This Example describes conjugation of an antibody to a cell surface.

An anti-PD-L1 antibody (aPD-L1) (rat IgG2b) was coupled to erythroid cells under different reaction conditions described in Table 4. To perform the reaction, erythroid cells were labeled with 0.1 mM 3-Azidopropionic Acid Sulfo-NHS ester (AS) (resuspended in DMSO) for a labeling concentration of 0.1 mM AS. aPD-L1 was labeled with 10× excess of DBCO-Sulfo-NHS ester (DS) (20 ul of 10 mM DS). The labeled cells were incubated with the concentration, volume and amount of the labeled aPD-L1 indicated in Table 4 for 1 hour at 25° C. The cells were then washed with PBS, and stained with an anti-rat kappa light chain antibody linked to a fluorophore (PE). The cells were then analyzed via flow cytometry to determine the protein labeling efficiency. As shown in Table 4, the protein labeling efficiency was determined to be in the range of 99.7-99.9%. A cell is considered positive for fluorescence if its fluorescence is greater than 99% of otherwise similar unlabeled cells. The number of aPD-L1 molecules present per cell was determined, and found to be 7000-15000 molecules of aPD-L1 per cell. The amount of protein (in ng) clicked per cell was also determined and is shown in Table 4. In general, adding higher concentrations of protein resulted in a higher percentage of cells being modified and a higher number of molecules conjugated per cell. This experiment demonstrates the production of a population of cells having a very high labeling efficiency with a protein, e.g., attaining an average number of molecules per cell in the range of 7000 to 14,000 molecules per cell. This experiment also demonstrates that a multimer can be linked to a cell, as the antibody has two heavy chains and two light chains. The experiment also indicates that large populations of cells, e.g., having 1E8 or 1E9 erythroid cells, can be labeled, with a high percentage of cells labeled and a desired amount of protein per cell achieved.

TABLE 4 Efficiency of labeling cells with aPD-L1 Number Volume Concentration % of of of Protein Cells Molecules/ Protein Cells Protein (mg/mL) Clicked Cell (ng) 1E7  10 ul 4.5 99.9 6,955 2.88 1E7  10 ul 2 99.8 7,014 2.91 1E7  10 ul 0.5 99.7 6,728 2.78 1E8  50 ul 4.5 99.9 13,892 57.61 1E8  50 ul 2 99.8 10,934 45.30 1E8  50 ul 0.5 99.7 9,797 40.55 1E9 100 ul 4.5 99.9 14,916 618.61 1E9 100 ul 2 99.8 12,126 502.40 1E9 100 ul 0.5 99.7 7,476 309.43

Example 5: Coupling of a Protein Ligand Agent to Erythroid Cells Via a Residual Linker Comprising a Click Signature

41BB ligand (m41BBL) was coupled to erythroid cells. To perform the reaction, erythroid cells were labeled with 3-Azidopropionic acid Sulfo-NHS Ester (AS) and m41BBL was labeled with DBCO-sulfo-NHS ester (DS). The labeled cells were incubated with 1-5 mg/ml of labeled m41BBL, in a volume of 10-30 μL, for 1 hour at 23° C. The cells were then washed with phosphate buffered saline with 0.1% bovine serum albumin, and stained with fluorescent detection reagent (anti-m41BBL-PE). The cells were then analyzed via flow cytometry to determine the protein clicking efficiency. As shown in Table 5, the protein clicking efficiency was determined to be in the range of 1.14-99.9%. A cell is considered positive for fluorescence if its fluorescence is greater than 99% of otherwise similar unlabeled cells. This experiment demonstrates the production of a population of cells having a very high labeling efficiency with a protein ligand.

TABLE 5 Efficiency of labeling cells with m41BBL Number m41BBL m41BBL Percent of concentration molecules/ cells positive cells (mg/ml) cell for fluorescence 1E7 1.024 44,158 88.7% 1E8 1.024 40,926 86.5% 1E8 5 94,874 99.9%

Example 6: A Protein Ligand Coupled to Erythroid Cells has Binding Activity

It is often desirable to produce a cell population having a high percentage of labeled cells, and a high level of clicked protein per cell. At the same time, it is usually desirable to avoid “over-labeling”, e.g., destroying a protein's functionality by conjugating linkers to too many sites on the protein. Consequently, functionalized erythroid cells having clicked proteins were tested for the ability to bind a physiological ligand.

41BB ligand (m41BBL) was coupled to erythroid cells as described in Example 5. The cells were then contacted with 41BB (the cognate binding partner of 41BBL), a Phycoerythrin-labeled antibody that binds 41BB, and an Allophycocyanin (APC)-labeled antibody that binds 41BB. Binding of the 41BB to the cells indicates that not only is 41BBL present on the cells, but that its binding site is functional and oriented to permit binding. Binding of the anti-41BBL antibody confirms that 41BBL is present on the cells. The cells were analyzed via flow cytometry to determine the protein labeling efficiency. As shown in Table 6, 41BB binding was determined to be in the range of 71.4-97.0%. A cell is considered positive for fluorescence if its fluorescence is greater than 99% of otherwise similar unlabeled cells. This experiment demonstrates the production of cells with very high labeling efficiency yet without “over-labeling”, e.g., without destroying the ligand's binding site.

TABLE 6 Binding of erythroid cell-m41BBL to 41BB Number m41BBL degree of Percent cells positive for of cells labeling w/DS fluorescence 1E7 ~2.64 71.4% 1E8 ~2.64 72.4% 1E8 ~1.74 97.0%

Example 7: An Antibody Coupled to Erythroid Cells has Binding Activity

It is often desirable to produce a cell population having a high percentage of labeled cells, and a high level of clicked protein per cell, without “over-labeling.” Consequently, a clicked antibody was tested for the ability to bind its antigen.

Anti-PD-L1 was coupled to erythroid cells. To perform the reaction, erythroid cells were labeled with 3-Azidopropionic acid Sulfo-NHS Ester (AS) and aPD-L1 was labeled with DBCO-sulfo-NHS ester (DS). The labeled cells were incubated with 2 mg/ml of labeled anti PD-L1, in a volume of 20 ul, for 1 hour at 20° C. The cells were then contacted with recombinant mouse PD-L1 having an Fc chimera tag. This can be detected with anti Fc antibody. Binding of the mouse erythroid cells that are clicked with aPD-L1 to the recombinant protein was demonstrated by a complete shift of the population so that all of the cells are double positive for rat antibody (indicating the presence of the antibody) as well as Fc tag (indicating binding to the recombinant protein).

Additionally, the ability of aPD-L1 labelled erythroid cells to bind to murine tumor cell lines that express PD-L1 was evaluated. Initially PD-L1 expression was evaluated in three cell lines: CT-26, B16F.10 and A20 with or without IFNg stimulation for 24 hr (which induces PD-L1 expression on the tumor cells). Expression of PD-L1 was evaluated by staining with aPD-L1 antibody in comparison with isotype control antibody. Binding of erythroid cells that are clicked with aPD-L1 to PD-L1 expressing cells was evaluated by incubating cancer cells that were prelabelled with cell trace Far red and erythroid cells at 4° C. for 2 hours. The cell suspension was stained with anti-Kappa chain antibody and assessed in flow cytometer. A population that is double positive for Far Red and kappa would indicated that the erythroid cells bound to tumor cells. This experiment evaluated conditions with or without IFNg pre-incubation and compared the aPD-L1 clicked erythroid cells to cells that are clicked with an isotype control antibody. The percentage of tumor cells that bound to aPD-L1 mouse erythroid cells ranged between 60-99% depending on the level of PD-L1 expression in the tumor cell line (FIG. 3). The percentage of tumor cells that bound to isotype control clicked mouse erythroid cells did not correlate with level of PD-L1 expression, as expected. Overall, the binding of aPD-L1 mouse erythroid cells to tumor cells was significantly enhanced with increased PD-L1 expression. Binding of erythroid cells expressing aPD-L1 to recombinant PD-L1 and to tumor cells expressing PD-L1 indicates that not only is anti-PD-L1 present on the cells, but that its binding site is functional and oriented to permit binding.

Example 8: Quantifying Unreacted Coupling Reagent on Cells and Proteins

In some embodiments, it is desirable to have no, or very low levels of, un-reacted click linker present on the cell and the protein to which it is linked. While not wishing to be bound by theory, in some embodiments, lower levels of un-reacted click linker are associated with lower immunogenicity of the functionalized cell. This example describes quantification of un-reacted click linker present on the cell and the protein.

Cells were labeled by reaction with 3-Azidopropionic acid Sulfo-NHS Ester (AS), and m41BBL protein was labeled by reaction with DBCO-sulfo-NHS ester (DS). The cells and protein were then combined to conjugate the protein to the cell surface. Residual unreacted linker was then detected by adding fluorescently labeled linker, wherein addition of Cy5 DBCO reacted with and identified residual linker on the cell, and addition of Cy5 biotin Azide reacted with and identified residual linker on the protein. The experiment indicated low levels of un-reacted linker on proteins, specifically 11.2%. This Example demonstrates the ability to detect previously unreacted linker sites on the manufactured cell and protein, e.g., as a quality control test. It also demonstrates the ability to reduce the number of unreacted linker sites on the manufactured cell and protein by reacting them with a linker, e.g., a linker with low steric hindrance.

Example 9: Conjugating Exogenous Polypeptide Agents onto Various Cell Types

A mixture of cells was obtained from mouse spleen by mechanical disruption and lysing red blood cells. The remaining cells were labeled with 0.1 mM 3-Azidopropionic acid Sulfo-NHS Ester (AS). Purified E. Coli asparaginase was labeled with DBCO. The labeled cells and protein were then combined to allow conjugation. Surface asparaginase was detected with a rabbit anti-asparaginase antibody and an anti-rabbit secondary antibody labeled with Alexa Fluor 657. The identity of each cell type was detected using the markers described in Table 7. The cells were analyzed by flow cytometry. The experiment indicated significant labeling of all cell types tested as indicated in Table 7, using a gating strategy designed to distinguish between different types of cells in the population.

TABLE 7 Labeling efficiency of different cell types Markers Cell Type Percent Clicked by Protein Detection CD3+ CD4+ CD4 T cells 99.1% CD3+ CD8+ CD8 T cells 99.2% CD3− NK1.1+ Natural Killer Cells 99.4% CD3+ NK1.1+ Natural Killer T cells 99.3% CD11b+ Myeloid Cells 89.4% CD11c+ Dendritic Cells 88.5% CD19+ CD61− B cells 95.0% CD61+ CD19− Platelets 96.7% CD11b− Ly6G++ Neutrophils 84.1%

The experiment also demonstrates conjugation of an enzyme to the surface of numerous cells, including immune cells, nucleated cells, and enucleated cells.

Example 10: Erythroid Cells Conjugated to an Exogenous Polypeptide Agent Slow Tumor Growth In Vivo

An MC38 mouse model system for colon cancer was used to test the effects of functionalized erythroid cells on tumor growth. Without being bound by theory, 41BBL is thought to slow tumor growth by eliciting diverse immune effector responses on both the innate and adaptive immune arms. The most potent responses stimulate CD8+ cytotoxic T cells to proliferate and increase their effector potential through increased interferon gamma production and expression of multiple granzymes. In contrast, published preclinical data using multiple 4-1BB agonists have shown little or no single agent antitumor activity in the MC38 or other models (Chen, et al, 2014; Kudo-Saito, et al, 2006; Kocak, et al, Canc Res 2006; Tirapu, et al, Int J Cancer 2004; John, et al, Canc Res 2012). These differences in activity suggest that recapitulating the cell-cell binding of 4-1BB effector cells (e.g. T cells, NK cells) using cellular presentation by 4-1BB-L-expressing erythroid cells is more effective in stimulating anti-tumor responses than agonist antibody-based approaches.

Cells were conjugated with 41BBL as described in Example 5. In this study, 94.7% of the cells were labelled with m4-1BB-L. The amount of molecules labelled per cell was quantified using flow cytometry. For dosing animals, there were an average of 1.1e9 m4-1BB-L mRBCs administered per dose with an average of 36,200 m4-1BB-L molecules per cell corresponding to 0.084 mg/kg m4-1BB-L per dose.

Fourteen female C57/B6 aged 6-8 weeks mice were inoculated s.c. in left flank with 5×10⁵ MC-38 cells. Animals' weights and condition were recorded daily, and tumors were measured 3 times per week.

Tumors were measured three times a week by measuring each tumor in 2 dimensions. Tumor volumes were calculated using the standard formula: (L×W²)/2. The mean tumor weight and standard error of the mean was calculated for each group at each time point.

The observed anti-tumor activity of m4-1BB-L mRBC compared to untreated controls is shown in FIG. 4 and demonstrates a reduction in tumor growth in mice treated with m4-1BB-L mRBC. Tumor volume distributions demonstrated statistically significant differences between the groups as early as day 5 of the study and up until day 9 (P<0.05, T test).

Body weight was recorded daily. Changes in body weight were calculated for each mouse relatively to the body weight recorded on day 1. Treatment was well tolerated as indicated by overall increase in body weight for most mice. Mice that showed some decrease in body weight, did not lose more than 5% of the total body weight throughout the study.

These data support a significant efficacy and potency advantage of cellular presentation of 4-1BB-L via erythroid cells over agonistic antibody approaches. Significant antitumor activity was observed with m4-1BB-L mRBC in the MC38 model that was not previously seen with a 4-1BB agonist antibody dosed at a 10-fold higher level than m4-1BB-L in the same model (Chen, et al, 2014). The increased potency and activity of m4-1BB-L mRBC compared to agonist antibody approaches is consistent with 4-1BB-L cellular presentation and a corresponding 4-1BB receptor multimerization that is required to induce potent signaling via 4-1BB (Bremer, 2013) and that would normally occur within the immune synapse.

Example 11: Erythroid Cells Comprising Three Exogenous Polypeptide Agents Covalently Linked to the Cell Surface by a Residual Linker Comprising a Click Signature

To test the ability to label cells with a plurality of agents, erythroid cells were functionalized with three different agents. The three agents (Factor VIIa, Factor Xa, and Cy5) were labeled with DBCO-sulfo-NHS ester (DS) or bought as DBCO labeled (i.e. Cy5). The cells were labeled with 3-Azidopropionic acid Sulfo-NHS Ester (AS). The labeled cells were the combined with the labeled agents to allow conjugation to occur. Presence of the three agents on the cells was detected by flow cytometry. The experiment indicated that 33.6% of cells were positive for all three of the agents.

Example 12: Agents Linked to Sugars

Agents can be linked directly to proteins on the cell surface, e.g., as described above. However, agents can also be linked to sugars on the cell surface, e.g., to glycan chains on glycoproteins as described in this Example. Cells having glycans at the cell surface are labeled with a bifunctional linker having one click handle and one group that reacts with a glycan.

In one approach, the click handle is added to the glycan using an adaptation of a commercially available kit developed for labeling glycans on antibodies. In this adaptation, the cells rather the antibody are first treated with endoglycosidase to hydrolyze glycans after the core GlcNAc. Then, the cells are washed and treated with an engineered galactosyl transferase, GalT(Y289L) and GalNAzide. The GalT attaches a GalNAzide residue to the exposed GlcNAc, resulting in an azide available for a biocompatible strain-promoted azide-alkyne chemistry reaction with an alkyne modified protein.

In another approach, sugar moieties within glycans are first modified to create aldehydes and ketones via a mild periodate-mediated oxidation of vicinal diols using methodology described in de Bank et al Biotechnol Bioeng 81: 800-808, 2003. An alkyne containing or azide containing click handle can then be added to the resulting aldehyde and ketone groups using alkyne hydrazide or ethymyl hydrazide, respectively. The agent can then be labeled with the corresponding azide or alkyne as described in other examples above. The labeled agent is then incubated with the labeled cells to allow conjugation to occur. Linkage of the agent to the cell can be detected by flow cytometry, e.g., as described above.

The linkage can also involve a sugar on the agent. For example, an agent (e.g., an exogenous protein or antibody) having a sugar can be labeled with a bifunctional linker having one click handle and one group that reacts with a glycan, e.g., one of the linkers described above. A cell can be labeled with a second linker, e.g., a linker that reacts with a protein or a sugar at the cell surface. The labeled cell and labeled agent are then mixed together to allow conjugation to occur. Linkage of the agent to the cell can be detected by flow cytometry, e.g., as described above.

Example 13: Measuring Immunogenicity of Functionalized Erythroid Cells

In some embodiments, functionalized erythroid cells have low immunogenicity. Immunogenicity can be tested by measurement of antibodies generated against a protein expressed on an erythroid or other cell. One standard method to measure these antibodies is using a direct ELISA. Immunogenicity against a protein or agent linked to the erythroid cell can be measured by administering the functionalized erythroid cell to an animal or patient and then obtaining plasma or serum samples over a period of days or weeks. Serial dilutions of the samples are prepared and then incubated for 10-120 minutes in ELISA plate wells that have been precoated with the protein or agent used to functionalize the erythroid cell so that any antibodies generated against the protein or agent can bind. Plates are then washed and incubated with enzyme-labeled (e.g. horseradish peroxidase) polyclonal antibodies that bind to any antibodies that have bound to protein or agent. The wells are then washed and the level of enzyme activity remaining in the well is measured to assess the level of antibodies raised against the protein or agent used to functionalize the erythroid cell.

Example 14: Functionalizing Erythroid Cells with an Erythroid Cell Cytotoxic Agent

This example describes how a cell can be functionalized with a toxic agent, e.g., an agent which if expressed in the erythroid cell would be toxic to it, e.g., an agent that reduces growth rate, viability, cell life span, or function (erythroid cell cytotoxic). Cytotoxic agents include, e.g., enzymatic proteins which degrade amino acids and impair the growth and expansion of a cell, enzymes which are involved in modifying or degrading key metabolic molecules or molecular intermediates, or proteins or molecules such as ricin that interfere with critical cellular processes.

One example of an erythroid cell cytotoxic agent is asparaginase, which is used clinically to starve cancer cells. Overexpression of asparaginase in maturing erythroid cells interferes with cell growth and cellular maturation.

Cells, e.g., murine red blood cells from B6.129S7-Rag1^(tm1Mom)IJ (Rag1 knockout mice), are labeled in vivo by injecting mice with 2 mg of 3-azidopropionic acid sulfo-NHS ester and then harvesting cells 2 days later.

A erythroid cell cytotoxic agent, e.g., asparaginase, is labeled with 5× and 2.5× molar excess of DBCO-sulfo-NHS ester for 30 minutes at 25° C. 5× molar excess of DBCO-sulfo-NHS ester leads to ˜2 labels per asparaginase monomer and 2.5× molar excess of DBCO-sulfo-NHS ester leads to ˜1.2 labels per asparaginase monomer.

The labeled cells are then combined with 2 different concentrations of asparaginase-labeled DBCO to different degrees for 60 minutes to allow conjugation to occur and attain cells labeled to different degrees. Presence of the agent on the surface of the cell can be detected using an activity assay for asparaginase, using flow cytometry with an antibody against asparaginase.

TABLE 8 Asparaginase activity of labeled cells Asparaginase activity Cell labeling reaction of labeled cells Higher 1e9 cells + 1.6 mg asparaginase 2.16e−10 units/cell degree of modified with ~2 labels/tetramer labeling Lower 1e9 cells + 0.2 mg asparaginase 4.32e−11 units/cell degree of modified with ~1.2 labels/tetramer labeling

The relative ability of the red blood cell conjugated asparaginase versus unconjugated asparaginase to deplete serum asparaginase over time can be tested in mice. Mice were injected with control red blood cells, RBC labeled with high or low amounts of asparaginase together, or with low, medium, or high amounts of unconjugated recombinant asparaginase as depicted in Table 9. Control and asparaginase conjugated RBCs were additionally labeled with a fluorescent tag, Cy5, to determine the pharmacokinetics of the RBCs following injection. Blood samples are then taken at various times after injection to determine the levels of asparagine and labeled RBCs levels.

TABLE 9 Set-up for injection of asparaginase-labeled cells in mice. Number Number Total units of Recipient of of cells Asparaginase mouse animals Description injected injected Group 1 C57BL/6 3 Cell not labeled with 1e9 — asparaginase Group 2 C57BL/6 3 Cells labeled with higher 1e9 0.22 dose of asparaginase Group 3 C57BL/6 3 Cells labeled with lower 1e9 0.043 dose of asparaginase Group 4 C57BL/6 3 2.8 ug recombinant — 0.19 asparaginase Group 5 C57BL/6 3 0.39 ug recombinant — 0.025 asparaginase Group 6 C57BL/6 3 15 ug recombinant — 0.97 asparaginase Group 7 B6.129S7- 3 Cell not labeled with 1e9 — Rag1^(tmlMom)IJ asparaginase Group 8 B6.129S7- 3 Cells labeled with higher 1e9 0.22 Rag1^(tmlMom)IJ dose of asparaginase Group 9 B6.129S7- 3 Cells labeled with lower 1e9 0.043 Rag1^(tmlMom)IJ dose of asparaginase Group 10 B6.129S7- 3 2.83 ug recombinant — 0.19 Rag1^(tmlMom)IJ asparaginase Group 11 B6.129S7- 3 0.385 ug recombinant — 0.025 Rag1^(tmlMom)IJ asparaginase

When 0.39, 2.8, or 15 micrograms of recombinant asparaginase was injected into C557BL/6 mice injected into mice, serum asparagine was reduced to near zero 6 hours after injection (FIG. 5). However, for the 0.39 ug group, serum asparagine levels rose to near normal levels by 1 day post injection, while the 2.8 and 15 ug dose groups rose near or above normal levels by day 4. In contrast, the asparagine levels were reduced to near zero from 6 hours out to 8 days in C57BL/6 mice dosed with either low or high amounts of asparaginase coupled to red blood cells with levels starting to rise again by day 11 (FIG. 5). Similar results were obtained in the Rag1 mice (FIG. 6); however, in contrast to the C57BL/6 mice, the asparagine levels remained near zero up to day 29 (FIG. 6). The pharmacokinetics of the ASNase conjugated cells is also measured by detecting the percentage of Cy5-positive cells at various times after injection using flow cytometry. One day after injection the clearance of the remaining ASNase-conjugated cells was similar to the Cy5-labeled cells (FIGS. 7A and 7B). Approximately 20% of the RBCs present in the circulation at day 1 remained in the blood by day 18. For cells with a higher level of ASNase, the initial rapid clearance of cells was larger than for the cells with lower levels of ASNase. Despite this initial rapid clearance, the cells remaining in the circulation after the first day remained detectable in the circulation to at least day 22. This experiment demonstrates that conjugating asparaginase to red blood cells dramatically improves the circulation time of asparaginase in the blood. This enhanced exposure is associated with a dramatic improvement in the ability to reduce serum asparagine levels over days and weeks with a single dose.

In addition, the pharmacokinetic profile for the asparaginase-labeled RBCs also did not change with repeated dosing, indicating a lack of immunogenic response to the asparaginase-labeled RBCs for all three levels of asparaginase, as detectable by this assay.

Example 15: Coupling of an Enzyme Agent to Erythroid Cells Via a Residual Linker Comprising a Click Signature

Factor Xa (FXa) was coupled to erythroid cells. To perform the reaction, 1e9-1.36e10 cell/ml erythroid cells were labeled with 3-Azidopropionic acid Sulfo-NHS Ester (AS) and FXa was labeled with DBCO-sulfo-NHS ester (DS). The labeled cells were incubated with 0.5-1.7 mg/ml of labeled FXa, in a volume of 10 μL-3 mL, for 1 hour at 23° C. The cells were then washed with phosphate buffered saline with 0.1% bovine serum albumin, and stained with fluorescent detection reagent (anti-FXa-PE). The cells were then analyzed via flow cytometry to determine the protein clicking efficiency. Protein clicking efficiency was determined to be in the range of 99%. This experiment demonstrates the production of a population of cells having a very high labeling efficiency with an enzyme.

The number of Factor Xa protein molecules per cell was quantified by antibody binding capacity to be 1,000-250,000 molecules per cell. The number of proteins per cell can be tuned, e.g., using protein concentration, number of cells, and reaction volume, e.g., as described in Example 4.

Activity of Factor Xa was quantified by TGA activity as up to 14,000 active molecules per cell.

Example 16: Coupling of Protein Agents to Human Erythroid Cells Via a Residual Linker Comprising a Click Signature

Factor Xa (FXa) and Asparaginase (ASNase) were coupled to human erythroid cells. To perform the reaction, erythroid cells were labeled with 3-Azidopropionic acid Sulfo-NHS Ester (AS) and FXa and ASNase was labeled with DBCO-PEG5-NHS ester (DP) and DBCO-sulfo-NHS ester (DS), respectively. The labeled cells were incubated with 1.03 mg/ml of labeled FXa and 4.535 mg/ml ASNase, in a volume of 10 μL, for 1 hour at 23° C. The cells were then washed with phosphate buffered saline with 0.1% bovine serum albumin, and stained with fluorescent detection reagent (anti-FX-PE and anti-ASNase-AlexaFluor 488). The cells were then analyzed via flow cytometry to determine the protein clicking efficiency. The protein clicking efficiency was determined to be in the range of 99.9% for FXa and 71.1% for ASNase. This experiment demonstrates the production of a population of human erythroid cells having a very high labeling efficiency with different proteins.

Example 17: Coupling of a Peptide Agent to Erythroid Cells Via a Residual Linker Comprising a Click Signature

Biotinylated myelin oligodendrocyte glycoprotein 35-55 (MOG) peptide was coupled to erythroid cells. To perform the reaction, erythroid cells were labeled with different amounts (high and low) of 3-Azidopropionic acid Sulfo-NHS Ester (AS) and MOG peptide was labeled with DBCO-sulfo-NHS ester (DS). The labeled cells were incubated with 2.7 mg/ml of labeled MOG-DBCO, in a volume of 10 μL, for 1 hour at 23° C. The cells were then washed with phosphate buffered saline with 0.1% bovine serum albumin, and stained with fluorescent detection reagent (anti-biotin-PE). The cells were then analyzed via flow cytometry to determine the peptide clicking efficiency. The peptide clicking efficiency was determined to be in the range of 67.4% to 91.8% for MOG. This experiment demonstrates the production of a population of cells having a tunable degree of labeling efficiency with peptide. This experiment also demonstrates that a short peptide (about 20 amino acids) can be efficiently clicked onto erythroid cells.

Example 18: Coupling of a Cytokine Agent to Erythroid Cells Via a Residual Linker Comprising a Click Signature

Human IL10 (hIL10) was coupled to erythroid cells. To perform the reaction, erythroid cells were labeled with 3-Azidopropionic acid Sulfo-NHS Ester (AS) and hIL10 was labeled with DBCO-sulfo-NHS ester (DS). The labeled cells were incubated with 0.24-0.79 mg/ml of labeled hIL10, in a volume of 2 μL, for 1-3 hours at 23° C. or 16 hours at 4° C. The cells were then washed with phosphate buffered saline with 0.1% bovine serum albumin, and stained with a fluorescent detection reagent (anti-hIL10-PE). The cells were then analyzed via flow cytometry to determine the protein clicking efficiency. As shown in Table 10, the protein clicking efficiency was determined to be in the range of 76.7-100%. A cell is considered positive for fluorescence if its fluorescence is greater than 99% of otherwise similar unlabeled cells. This experiment demonstrates the production of a population of cells having a very high labeling efficiency, e.g., over 200,000 molecules per cell.

TABLE 10 Efficiency of labeling cells with hIL10 Number hIL 10 Click hIL10 Percent of concentration reaction molecules/ cells positive cells (mg/ml) time (hours) cell for fluorescence 4E7 0.79 1 69,964 76.7% 4E7 0.79 3 128,766 99.9% 4E7 0.24 16 158,572 99.9% 4E7 0.583 1 208,519  100%

Example 19: A Cytokine Coupled to Erythroid Cells has Binding Activity

Functionalized erythroid cells having clicked proteins were tested for the ability to bind a physiological ligand. As discussed above, it is often desirable to have a high percentage of labeled cells and a high level of clicked protein per cell while preserving the protein's binding activity.

Human IL10 (hIL10) was coupled to erythroid cells as described in Example 18. The cells were then contacted with human IL10 receptor alpha Fc fusion (the cognate binding partner of hIL10), an allophycocyanin (APC)-labeled antibody that binds Fc was used to detect interaction of hIL10 clicked onto cells and its binding to human IL10 receptor alpha. Binding of the hIL10 receptor alpha to the cells indicates that not only is hIL10 present on the erythroid cells, but that its binding site is functional and oriented to permit binding. The cells were analyzed via flow cytometry to determine the protein labeling efficiency. As shown in Table 11, hIL10 binding was determined to be in the range of 90.0-95.0%. A cell is considered positive for fluorescence if its fluorescence is greater than 99% of otherwise similar unlabeled cells. This experiment demonstrates the production of cells with very high labeling efficiency yet without “over-labeling”, e.g., without destroying the ligand's binding site.

TABLE 11 Binding of erythroid cell-hIL10 to hIL10 receptor alpha Number hIL10 degree of Percent cells positive for of cells labeling w/DS fluorescence 5E6 ~0.63 93.3% 5E6 ~1.39 95.0% 1E7 ~0.43 90.0%

Example 20: Coupling of a Cytokine in Combination with Targeting Moiety to Erythroid Cells

Human IL10 (hIL10) in combination with an anti-α4β7 Fab was coupled to erythroid cells. To perform the reaction, erythroid cells were labeled with 3-Azidopropionic acid Sulfo-NHS Ester (AS), hIL10 and anti-α4β7 Fab were individually labeled with DBCO-sulfo-NHS ester (DS). The labeled cells were incubated with 0.583 mg/ml of labeled hIL10, in a volume of 30 μL, and with 2.434 mg/ml of labeled anti-α4β7 Fab, in a volume of 19.35 μL, for 2 hours at 23° C. The cells were then washed with phosphate buffered saline with 0.1% bovine serum albumin, and stained with fluorescent detection reagents (anti-hIL10-BV421 and anti-rat kappa light chain-PE). The cells were then analyzed via flow cytometry to determine the protein clicking efficiency. The dual protein clicking efficiency was determined to be approximately 98.3%. A cell is considered positive for fluorescence if its fluorescence is greater than 99% of otherwise similar unlabeled cells. This experiment demonstrates the production of a population of cells having a very high labeling efficiency with a cytokine and a targeting moiety.

Example 21: Click Specificity

This Example demonstrates the specificity of click labeling. Three samples were assayed. First, untreated murine red blood cells (lacking a click handle) were mixed with a protein agent (anti-α4b7 Fab) having a DBCO click handle. Second, murine red blood cells having an azide click handle were mixed with an anti-α4b7 Fab that lacked a click handle. Third, murine red blood cells having an azide click handle were mixed with an anti-α4b7 Fab having a compatible DBCO click handle. The reactions were allowed to proceed for 1 hour at room temperature in PBS. The cells were then assayed for presence of the anti-α4b7 Fab by contacting them with an anti-rat IgG Kappa conjugated with PE (phycoerythrin) antibody and performing flow cytometry. A cell was considered positive for fluorescence if its signal was greater than that of 99% of untreated, otherwise similar cells in the presence of the detection reagent, but in the absence of anti-α4b7 Fab protein. As expected, the first and second samples had low fluorescence (1.81% and 1.53% of the cells fluoresced, respectively), while the third sample was highly fluorescent (95.2% of the cells fluoresced). This example demonstrates that click labeling is highly specific.

Example 22: Conjugation of a Click Handle to the N-Terminus of an Agent

It is often desirable to prevent disruption of protein biology, for example, by biasing labeling towards the N-terminus of a protein of interest, e.g., to better preserve functionality of a C-terminal domain. Proteins of interest were prepared for coupling to erythroid cells by labeling with a coupling reagent. To better preserve the functionality of human IL10, NHS ester chemistry was biased towards N-terminal labeling. Proteins were desalted, and buffer was exchanged to PBS and then concentrated to ≥1 mg/mL prior to labeling. The pH maintained at neutral pH, approximately 7-7.4.

Stock solutions of coupling reagents were prepared as described in Example 1. The coupling reagent was added at a 1-to-1 molar ratio relative to the protein concentration. The protein labeling reaction was incubated at room temperature for 1 hour to 1 hour and 30 minutes, with gentle agitation every 10 minutes. In order to detect the level of labeling, the Nanodrop UV-Vis program was used to read approximately 1-3 μL of labeled protein at absorbance 280 nm and 309 nm with a baseline correction at 750 nm. Degree of labeling ranged from 0.63-1.39 DBCO click handle molecules per protein.

Example 23: Conjugation of a Click Handle to an Agent Comprising a Free Cysteine Residue, e.g., Situated in a n-Clamp, Using Maleimide Chemistry

It can be desirable to better preserve protein biology, for example, by introducing a free cysteine into a protein of interest for site specific maleimide chemistry conjugation. Proteins of interest (e.g., mouse 41BBL) were prepared for coupling to erythroid cells by labeling with a coupling reagent. To better preserve the protein functionality, a free cysteine was introduced into the recombinant 41BBL protein in the four amino acid sequence (FCPF, SEQ ID NO: 64) known as a “π-clamp” for site specific maleimide chemistry conjugation. Although a π-clamp is used in this example, it is contemplated that any free cysteine residue may be used for site specific conjugation, e.g., as described herein. Proteins were desalted, buffer exchanged to PBS, and concentrated to ≥1 mg/mL prior to labeling. Proteins were reduced with 1 mM DTT, incubated for 1 hour at room temperature, and desalted on a NAPS column.

The maleimide coupling reagent was added at a 5 fold molar excess relative to the protein concentration. The protein labeling reaction was incubated at room temperature for 4 hours and desalted using a NAP10 column. In order to detect the level of labeling, the Nanodrop UV-Vis program was used to read approximately 1-3 μL of labeled protein at absorbance 280 nm and 309 nm with a baseline correction at 750 nm. Degree of labeling ranged from 6-7.6 DBCO click handle molecules per protein.

Example 24: Conjugation of a Click Handle to an Agent Comprising Two Cysteine Residues, Using ThioLinker Chemistry

It can be desirable to introduce a click handle at a specific site in a protein of interest and/or in a particular orientation. Proteins of interest were prepared for coupling to erythroid cells by labeling with a coupling reagent. In one method, ThioLinker chemistry was introduced to recombinant anti-CTLA4 Fab protein for site specific click handle conjugation through bridging a disulfide bond. Fabs were desalted, buffer exchanged to PBS, and concentrated to ≥1 mg/mL prior to labeling. Fabs were then reduced with 5 mM DTT, incubated for 1 hour at 37° C., and then buffer exchanged into PBS. The ThioLinker coupling reagent was added at a 15 fold molar excess relative to the protein concentration to label the reduced disulfide bond. The protein labeling reaction was incubated at 4° C. for 16-18 hours and desalted using a Zeba column. In order to detect the level of labeling, the Nanodrop UV-Vis program was used to read approximately 1-3 μL of labeled protein at absorbance 280 nm and 309 nm with a baseline correction at 750 nm. Degree of labeling was 8.3 DBCO click handle molecules per protein. ThioLinker oriented click handle labeling on anti-CTLA-4 Fab was compared to other click handle reagents and found to result in substantial labeling of cells. ThioLinker-labeled anti-CTLA-4 was also found to significantly increase functional binding to recombinant CTLA4.

In another method, ThioLinker chemistry was used to site specifically label a recombinant protein (HIS6 mouse 41BBL) through the HIS6 purification tag. Proteins were typically desalted, buffer exchanged to PBS, and concentrated to ≥1 mg/mL prior to labeling. The ThioLinker coupling reagent was then added at a 20 fold molar excess relative to the protein concentration to label the HIS6 tag of the protein (non-reduced). The protein labeling reaction was incubated at room temperature for 3 hours and buffer exchanged to PBS using a Zeba desalting column. ThioLinker labeling of HIS6 mouse 41BBL clicked onto AS-labeled RBC resulted in increased functional ability for 41BBL-clicked cells to activate immune cells, as shown by IL-2 production (FIG. 8A) and interferon-γ (IFN-γ) production (FIG. 8B), respectively. It was observed that oriented linkage of HIS6 mouse 41BBL resulted in substantially greater IL-2 and IFN-γ secretion compared to random linkage, although the latter induced significantly greater cytokine secretion than click CTL control (AS-labeled RBCs only).

Example 25: Production of an Agent Comprising a Non-Canonical Amino Acid (ncAA)

It can be desirable to introduce a coupling reagent at a specific site of interest within a protein of interest, for example, by incorporating non-canonical amino acids (ncAA) into a protein of interest in a site-specific manner. In this example, proteins of interest were produced through co-transfection of Expi293 cells with a plasmid containing a tRNA/amino-acyl-tRNA synthase pair and a plasmid encoding the protein of interest (mIg-mouse 41BBL) with an amber stop codon (TAG) incorporated at a site of interest. Cells were plated and plasmids were transfected at 1.5 μg/mL of each plasmid using the ExpiFectamine kit on day 1. Different concentrations (2 mM, 1.3 mM, 1 mM, 250 μM) of ncAA (Exo(BCN)-Lys; FIG. 9A) were added to the transfected cells for site specific incorporation in place of the amber stop codon the same day. At day 3 after transfection, media was harvested to obtain secreted proteins. Secreted proteins were confirmed to have site specific ncAA incorporation through incubation with Azide-Biotin Cy5 for 30 min at room temperature and then western blot analysis. Proteins were detected with an anti-41BBL antibody and a secondary HRP antibody, and click handle incorporation was detected with an anti-biotin-HRP antibody.

TABLE 12 Proteins clicked Protein Labeling chemistry Ovalbumin DBCO-Sulfo-NHS ester Erwinase (Erwinia asparaginase) DBCO-Sulfo-NHS ester Uricase DBCO-Sulfo-NHS ester Lysozyme DBCO-Sulfo-NHS ester Anti-CTLA4 Fab ThioLinker-DBCO Anti-CD3 Fab ThioLinker-DBCO Anti-PDL1 Fab ThioLinker-DBCO

As shown in FIG. 9B, site-specific incorporation of the ncAA exo(BCN)-lysine resulted in the production of clickable murine 41BBL.

Example 26: Coupling of Urate Oxidase to Erythroid Cells Via a Linker Having a Click Signature

Recombinant Candida utilis His₆-urate oxidase was expressed and purified from E. coli and labeled with DBCO-sulfo-NHS ester yielding urate oxidase at a ratio of approximately 1 label per monomer. Murine red blood cells (RBCs) were labeled with 6-Azidohexanoic Acid Sulfo-NHS ester. Coupling reactions were performed in which 1e9 labeled murine RBCs were incubated in the presence of either 0 uM or 75 uM DBCO-labeled urate oxidase for 2 hours at room temperature. The degree of urate oxidase conjugation was evaluated by staining the murine RBCs for His₆-urate oxidase with DyLight 488-labeled anti-His₆ antibody, followed by flow cytometry analysis. 100% of the RBCs incubated with 75 uM urate oxidase were labeled with the enzyme; in contrast only 0.16% of negative control cells treated with 0 uM urate oxidase showed positive fluorescence in this assay. The RBCs coupled to urate oxidase were able to efficiently deplete uric acid, showing a urate oxidase activity of about 4.6e-12 units/cell.

Example 27: Erythroid Cells Comprising Exogenous Polypeptide Agent are Active In Vivo

Enucleated erythroid cells were conjugated with anti-PD-L1 at their surface and tested for the ability to infiltrate tumors in mice.

Mice were inoculated with B16F10 cells SC. Tumors were allowed to grow to 400 cubic mm before dosing. Murine RBC were conjugated with fragments antibody (Fab) from anti murine PD-L1 and isotype control. Conjugated murine RBC were labeled with CTFR according to the manufacturer's protocol. Cells were infused into the animals. One day after infusion, tumors were collected. Tumors were sectioned and stained with anti CD31 to visualize tumor vasculature and DAPI to visualize nuclei. Stained sections were scanned and pictures were taken. Using Halo software, the tumor areas and vasculature areas were identified. Total cell counts of labeled RBC in these two areas were taken for both isotype control and anti-PD-L1. The ratio between the RBC found in the tumor and the RBC found in the vessels was calculated. The ratio between RBC in the vessels and RBC in the tumor is 1 (average of measurement in tumors from 8 mice) for the isotype control conjugated RBC, indicating similar amounts in the tumor and the vasculature. The ratio between RBC in the vessel and RBC in the tumor is 1.7 for the anti PD-L1 treated mice, indicating enrichment of RBC in the tumor in the anti-PD-L1 group in comparison with the isotype control mice. The difference in ratio between the 2 groups was statistically significant with P<0.01 (student T test).

While not wishing to be bound by theory, tumors expressing higher levels of PD-L1 may respond better to RCTs comprising anti-PD-L1 than tumors that express lower levels of PD-L1. The B16F10 cells expressed about 300,000 copies per cell of PD-L1 when stimulated with IFN-gamma at 10 ng/ul. In contrast, CT26 cells expressed about 150,000 copies per cell of PD-L1 and A20 cells expressed about 100,000 copies per cell of PD-L1 under the same conditions. PD-L1 copy number was measured using a Quantum Simply Cellular kit (Bangs Laboratories).

Erythroid cells comprising an anti-PD-L1 antibody at their surface showed greater binding to the IFN-gamma treated B16F10 cells and CT26 than to the A20 cells, consistent with greater levels of PD-L1 expression on the tumor cells leading to increased binding of the erythroid cells to the tumor cells. 

What is claimed is:
 1. An enucleated erythroid cell, comprising an exogenous polypeptide agent covalently linked to the cell surface by a residual linker comprising a click signature, via an amino acid side chain of a protein at the cell surface, wherein the click signature was formed as the product of a click reaction or has the structure of a click signature.
 2. An enucleated erythroid cell, comprising: a plurality of exogenous polypeptide agents, each exogenous polypeptide agent of the plurality being covalently linked to the cell surface by a residual linker comprising a click signature, wherein at least 10% of exogenous polypeptide agents on the cell are linked via an amino acid side chain to a protein at the cell surface, wherein the click signature was formed as the product of a click reaction or has the structure of a click signature.
 3. The enucleated erythroid cell of claim 2, wherein at least 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 99% of exogenous polypeptide agents on the cell are linked via an amino acid side chain to a protein at the cell surface.
 4. The enucleated erythroid cell of any of the preceding claims, which is not genetically engineered.
 5. The enucleated erythroid cell of any of the preceding claims, which does not comprise a non-natural amino acid.
 6. The enucleated erythroid cell of any of the preceding claims, wherein the exogenous polypeptide agent comprises a n-clamp.
 7. The enucleated erythroid cell of claim 6, wherein the exogenous polypeptide agent is covalently linked to the enucleated erythroid cell via the π-clamp.
 8. The enucleated erythroid cell of any of the preceding claims, wherein the exogenous polypeptide agent comprises a non-canonical amino acid (ncAA).
 9. The enucleated erythroid cell of claim 8, wherein the exogenous polypeptide agent is covalently linked to the enucleated erythroid cell via the ncAA.
 10. The enucleated erythroid cell of any of the preceding claims, which lacks a sortase transfer signature.
 11. The enucleated erythroid cell of claim any of the preceding claims, wherein the exogenous polypeptide agent is selected from an alpha4beta7 antibody, IL10, an enzyme such as asparaginase, or a clotting factor such as Factor Xa.
 12. The enucleated erythroid cell of any of the preceding claims, which comprises at least about 5,000, 10,000, 50,000, 100,000, or 200,000 copies of the exogenous polypeptide agent, or between 5,000-10,000, 10,000-50,000, 50,000-100,000, or 100,000-200,000 copies of the exogenous polypeptide agent.
 13. The enucleated erythroid cell of any of the preceding claims, wherein the exogenous polypeptide agent is a peptide ligand that binds a binding partner.
 14. The enucleated erythroid cell of any of the preceding claims, which has a clearance rate wherein at least 20% of the agent remains in the circulatory system of the subject over 1, 2, 3, 4, 5, 6, or 7 days.
 15. The enucleated erythroid cell of any of the preceding claims, wherein less than 10% of coupling reagent on the cell is unreacted coupling reagent.
 16. The enucleated erythroid cell of any of the preceding claims, which further comprises a second exogenous polypeptide agent, e.g., wherein the second exogenous polypeptide agent is covalently linked to the cell surface by a second residual linker comprising a click signature.
 17. The enucleated erythroid cell of claim 16, which further comprises a third exogenous polypeptide agent, e.g., wherein the third exogenous polypeptide agent is covalently linked to the cell surface by a second residual linker comprising a click signature.
 18. The enucleated erythroid cell of any of the preceding claims, wherein at least 50%, 60%, 70%, 80%, or 90% of the exogenous polypeptide agents are covalently linked to the cell surface with a preselected orientation, e.g., are attached by the same moiety of the exogenous polypeptide agents (e.g., an N-terminus, a C-terminus, or a particular residue, e.g., a cysteine).
 19. The enucleated erythroid cell of any of the preceding claims, wherein the exogenous polypeptide agent is covalently linked to an endogenous molecule of the cell, e.g., an endogenous polypeptide at the cell surface.
 20. A preparation comprising at least 10¹⁰, 10¹¹, or 10¹² enucleated erythroid cells of any of the preceding claims.
 21. The preparation of claim 20, wherein at least 70% of the enucleated erythroid cells in the preparation comprise the agent.
 22. The preparation of claim 20 or 21 wherein at least 70% of the enucleated erythroid cells in the preparation comprise an exogenous polypeptide agent that binds a ligand, e.g., in a flow cytometry assay of Example
 6. 23. The preparation of any of claims 20-22 wherein at least 50%, 60%, 70%, 80%, or 90% of the exogenous polypeptide agents in the preparation are covalently linked to an enucleated erythroid cell surface with a preselected orientation, e.g., are attached by the same moiety of the exogenous polypeptide agents (e.g., an N-terminus, a C-terminus, or a particular residue, e.g., a cysteine).
 24. A method of making an enucleated erythroid cell functionalized with an agent comprising: (a) providing an activated cell comprising a cell covalently bound to a first click handle, (b) providing an activated agent comprising an agent (e.g., an exogenous polypeptide) covalently bound to a second click handle capable of reacting with the first click handle, and (c) contacting the activated cell with the activated agent, thereby producing a cell functionalized with the agent.
 25. An enucleated erythroid cell produced by the method of claim
 24. 26. A method of administering an agent to a human subject, comprising administering an effective number of cells of any of claims 1-19 to the human subject, thereby administering the agent to the human subject.
 27. A cell of any of claims 1-19 for use as a medicament. 